nsv3921598

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:137,922,077
  • Description:GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 297763 SVs from 144 studies. See in: genome view    
Submitted genomic203,861-138,125,937Question Mark
Overlapping variant regions from other studies: 298285 SVs from 144 studies. See in: genome view    
Submitted genomic203,861-141,020,389Question Mark
Overlapping variant regions from other studies: 94940 SVs from 46 studies. See in: genome view    
Submitted genomic193,861-140,140,210Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeAssemblyAssembly UnitSequence IDChrInner StartInner Stop
nsv3921598Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9203,861138,125,937
nsv3921598Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9203,861141,020,389
nsv3921598Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000009.10Chr9193,861140,140,210

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15148176copy number gainMultipleMultipleSee casesPathogenicClinVarRCV000141876.43

Variant Call Placement Information

Variant Call IDPlacement TypeHGVSAssemblySequence IDChrInner StartInner Stop
nssv15148176Submitted genomicNC_000009.12:g.(?_
203861)_(138125937
_?)dup
GRCh38 (hg38)NC_000009.12Chr9203,861138,125,937
nssv15148176Submitted genomicNC_000009.11:g.(?_
203861)_(141020389
_?)dup
GRCh37 (hg19)NC_000009.11Chr9203,861141,020,389
nssv15148176Submitted genomicNC_000009.10:g.(?_
193861)_(140140210
_?)dup
NCBI36 (hg18)NC_000009.10Chr9193,861140,140,210

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15148176GRCh37: NC_000009.11:g.(?_203861)_(141020389_?)dup, GRCh38: NC_000009.12:g.(?_203861)_(138125937_?)dup, NCBI36: NC_000009.10:g.(?_193861)_(140140210_?)dupcopy number gainnot providedSee casesPathogenicClinVarRCV000141876.43

No genotype data were submitted for this variant

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