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nsv6960684

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,417,938

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3600 SVs from 87 studies. See in: genome view    
    Submitted genomic62,287,754-63,705,691Question Mark
    Overlapping variant regions from other studies: 3600 SVs from 87 studies. See in: genome view    
    Remapped(Score: Perfect):62,579,953-63,997,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6960684Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1562,287,75463,705,691
    nsv6960684RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1562,579,95363,997,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18395027deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18395027Submitted genomicNC_000015.10:g.622
    87754_63705691del
    GRCh38 (hg38)NC_000015.10Chr1562,287,75463,705,691
    nssv18395027RemappedPerfectNC_000015.9:g.6257
    9953_63997890del
    GRCh37.p13First PassNC_000015.9Chr1562,579,95363,997,890

    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)
    nssv183950274e-061276258
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