nsv3959229

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61,566

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 564 SVs from 68 studies. See in: genome view    
Submitted genomic32,787,838-32,849,403Question Mark
Overlapping variant regions from other studies: 564 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):32,755,615-32,817,180Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv3959229Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr632,787,83832,849,403
nsv3959229RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr632,755,61532,817,180

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15211908deletionOptical mappingOptical mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv15211908Submitted genomicNC_000006.12:g.(32
787838_?)_(?_32849
403)del
GRCh38 (hg38)NC_000006.12Chr632,787,83832,849,403
nssv15211908RemappedPerfectNC_000006.11:g.(32
755615_?)_(?_32817
180)del
GRCh37.p13First PassNC_000006.11Chr632,755,61532,817,180

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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