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nsv6657817

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80,021

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 301 SVs from 51 studies. See in: genome view    
    Submitted genomic9,699,745-9,779,765Question Mark
    Overlapping variant regions from other studies: 301 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):9,759,803-9,839,823Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6657817Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr19,699,7459,779,765
    nsv6657817RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr19,759,8039,839,823

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642523duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642523Submitted genomicNC_000001.11:g.969
    9745_9779765dup
    GRCh38 (hg38)NC_000001.11Chr19,699,7459,779,765
    nssv18642523RemappedPerfectNC_000001.10:g.975
    9803_9839823dup
    GRCh37.p13First PassNC_000001.10Chr19,759,8039,839,823

    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)
    nssv186425234e-061275952
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