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nsv5465230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
Submitted genomic116,121,762-116,121,836Question Mark
Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):116,442,925-116,442,999Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6116,121,762116,121,836
nsv5465230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6116,442,925116,442,999

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16987436duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16987436Submitted genomicNC_000006.12:g.116
121762_116121836du
p
GRCh38 (hg38)NC_000006.12Chr6116,121,762116,121,836
nssv16987436RemappedPerfectNC_000006.11:g.116
442925_116442999du
p
GRCh37.p13First PassNC_000006.11Chr6116,442,925116,442,999

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16987436<0.00116404
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