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nsv6559350

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:647

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 20 studies. See in: genome view    
    Submitted genomic140,094,614-140,095,260Question Mark
    Overlapping variant regions from other studies: 108 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):139,794,414-139,795,060Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6559350Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7140,094,614140,095,260
    nsv6559350RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7139,794,414139,795,060

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18274431inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18274431Submitted genomicNC_000007.14:g.140
    094614_140095260in
    v
    GRCh38 (hg38)NC_000007.14Chr7140,094,614140,095,260
    nssv18274431RemappedPerfectNC_000007.13:g.139
    794414_139795060in
    v
    GRCh37.p13First PassNC_000007.13Chr7139,794,414139,795,060

    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)
    nssv18274431<0.001235592
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