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nsv4342388

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,230

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 40 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):121,327,826-121,329,055Question Mark
Overlapping variant regions from other studies: 40 SVs from 7 studies. See in: genome view    
Submitted genomic120,967,880-120,969,109Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4342388RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7121,327,826121,329,055
nsv4342388Submitted genomicGRCh37.p13Primary AssemblyNC_000007.13Chr7120,967,880120,969,109

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15791215sequence alterationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15791215RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7121,327,826121,329,055
nssv15791215Submitted genomicGRCh37.p13NC_000007.13Chr7120,967,880120,969,109

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)
nssv157912154.6e-005121694
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