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nsv6905484

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:440,487

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1718 SVs from 95 studies. See in: genome view    
    Submitted genomic107,589,747-108,030,233Question Mark
    Overlapping variant regions from other studies: 1718 SVs from 95 studies. See in: genome view    
    Remapped(Score: Perfect):107,460,473-107,900,959Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11107,589,747108,030,233
    nsv6905484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11107,460,473107,900,959

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581581duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581581Submitted genomicNC_000011.10:g.107
    589747_108030233du
    p
    GRCh38 (hg38)NC_000011.10Chr11107,589,747108,030,233
    nssv18581581RemappedPerfectNC_000011.9:g.1074
    60473_107900959dup
    GRCh37.p13First PassNC_000011.9Chr11107,460,473107,900,959

    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)
    nssv185815814e-061275710
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