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nsv6176956

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:287

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 230 SVs from 42 studies. See in: genome view    
Submitted genomic157,749,673-157,749,959Question Mark
Overlapping variant regions from other studies: 230 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):157,542,365-157,542,651Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6176956Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7157,749,673157,749,959
nsv6176956RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7157,542,365157,542,651

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17905827deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17905827Submitted genomicNC_000007.14:g.157
749673_157749959de
l
GRCh38 (hg38)NC_000007.14Chr7157,749,673157,749,959
nssv17905827RemappedPerfectNC_000007.13:g.157
542365_157542651de
l
GRCh37.p13First PassNC_000007.13Chr7157,542,365157,542,651

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)
nssv179058270.00242238
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