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nsv6977577

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,389

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 27 studies. See in: genome view    
    Submitted genomic95,266,593-95,284,981Question Mark
    Overlapping variant regions from other studies: 100 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):95,732,930-95,751,318Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977577Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1495,266,59395,284,981
    nsv6977577RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1495,732,93095,751,318

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18392043deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18392043Submitted genomicNC_000014.9:g.9526
    6593_95284981del
    GRCh38 (hg38)NC_000014.9Chr1495,266,59395,284,981
    nssv18392043RemappedPerfectNC_000014.8:g.9573
    2930_95751318del
    GRCh37.p13First PassNC_000014.8Chr1495,732,93095,751,318

    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)
    nssv183920434e-061276260
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