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nsv6972520

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,843

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 78 SVs from 19 studies. See in: genome view    
    Submitted genomic64,805,402-64,808,244Question Mark
    Overlapping variant regions from other studies: 78 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):65,272,120-65,274,962Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972520Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,805,40264,808,244
    nsv6972520RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,272,12065,274,962

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18388581deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18388581Submitted genomicNC_000014.9:g.6480
    5402_64808244del
    GRCh38 (hg38)NC_000014.9Chr1464,805,40264,808,244
    nssv18388581RemappedPerfectNC_000014.8:g.6527
    2120_65274962del
    GRCh37.p13First PassNC_000014.8Chr1465,272,12065,274,962

    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)
    nssv183885814e-061276152
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