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nsv6925434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,698

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 27 studies. See in: genome view    
    Submitted genomic64,388,529-64,395,226Question Mark
    Overlapping variant regions from other studies: 120 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):64,782,309-64,789,006Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6925434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1264,388,52964,395,226
    nsv6925434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1264,782,30964,789,006

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371102deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371102Submitted genomicNC_000012.12:g.643
    88529_64395226del
    GRCh38 (hg38)NC_000012.12Chr1264,388,52964,395,226
    nssv18371102RemappedPerfectNC_000012.11:g.647
    82309_64789006del
    GRCh37.p13First PassNC_000012.11Chr1264,782,30964,789,006

    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)
    nssv183711027e-062276206
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