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nsv6467885

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106,251

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1618 SVs from 102 studies. See in: genome view    
    Submitted genomic7,763,859-7,870,109Question Mark
    Overlapping variant regions from other studies: 1618 SVs from 102 studies. See in: genome view    
    Remapped(Score: Perfect):7,916,455-8,022,705Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6467885Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,763,8597,870,109
    nsv6467885RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr127,916,4558,022,705

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18004465deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18004465Submitted genomicNC_000012.12:g.776
    3859_7870109del
    GRCh38 (hg38)NC_000012.12Chr127,763,8597,870,109
    nssv18004465RemappedPerfectNC_000012.11:g.791
    6455_8022705del
    GRCh37.p13First PassNC_000012.11Chr127,916,4558,022,705

    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)
    nssv18004465<0.001139126
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