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nsv6652410

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,994

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 41 studies. See in: genome view    
    Submitted genomic63,981,430-63,984,423Question Mark
    Overlapping variant regions from other studies: 150 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):64,447,102-64,450,095Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6652410Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr163,981,43063,984,423
    nsv6652410RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr164,447,10264,450,095

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18410288deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18410288Submitted genomicNC_000001.11:g.639
    81430_63984423del
    GRCh38 (hg38)NC_000001.11Chr163,981,43063,984,423
    nssv18410288RemappedPerfectNC_000001.10:g.644
    47102_64450095del
    GRCh37.p13First PassNC_000001.10Chr164,447,10264,450,095

    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)
    nssv184102884e-061275824
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