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nsv6776614

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:643,801

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1529 SVs from 78 studies. See in: genome view    
    Submitted genomic62,924,623-63,568,423Question Mark
    Overlapping variant regions from other studies: 1529 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):62,220,450-62,864,250Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6776614Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr562,924,62363,568,423
    nsv6776614RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr562,220,45062,864,250

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18512629deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18512629Submitted genomicNC_000005.10:g.629
    24623_63568423del
    GRCh38 (hg38)NC_000005.10Chr562,924,62363,568,423
    nssv18512629RemappedPerfectNC_000005.9:g.6222
    0450_62864250del
    GRCh37.p13First PassNC_000005.9Chr562,220,45062,864,250

    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)
    nssv185126294e-061275800
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