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nsv6571756

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:988

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 190 SVs from 26 studies. See in: genome view    
    Submitted genomic156,973,444-156,974,431Question Mark
    Overlapping variant regions from other studies: 190 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):156,766,138-156,767,125Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6571756Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7156,973,444156,974,431
    nsv6571756RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7156,766,138156,767,125

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18273793inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18273793Submitted genomicNC_000007.14:g.156
    973444_156974431in
    v
    GRCh38 (hg38)NC_000007.14Chr7156,973,444156,974,431
    nssv18273793RemappedPerfectNC_000007.13:g.156
    766138_156767125in
    v
    GRCh37.p13First PassNC_000007.13Chr7156,766,138156,767,125

    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)
    nssv18273793<0.001333810
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