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nsv6719560

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:237,705

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 800 SVs from 76 studies. See in: genome view    
    Submitted genomic20,401,562-20,639,266Question Mark
    Overlapping variant regions from other studies: 800 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):20,403,185-20,640,889Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6719560Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr420,401,56220,639,266
    nsv6719560RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr420,403,18520,640,889

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18495737deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18495737Submitted genomicNC_000004.12:g.204
    01562_20639266del
    GRCh38 (hg38)NC_000004.12Chr420,401,56220,639,266
    nssv18495737RemappedPerfectNC_000004.11:g.204
    03185_20640889del
    GRCh37.p13First PassNC_000004.11Chr420,403,18520,640,889

    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)
    nssv184957374e-061276254
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