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nsv6943400

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,617

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 13 studies. See in: genome view    
    Submitted genomic102,364,626-102,366,242Question Mark
    Overlapping variant regions from other studies: 153 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):103,016,976-103,018,592Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6943400Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13102,364,626102,366,242
    nsv6943400RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13103,016,976103,018,592

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18601263duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18601263Submitted genomicNC_000013.11:g.102
    364626_102366242du
    p
    GRCh38 (hg38)NC_000013.11Chr13102,364,626102,366,242
    nssv18601263RemappedPerfectNC_000013.10:g.103
    016976_103018592du
    p
    GRCh37.p13First PassNC_000013.10Chr13103,016,976103,018,592

    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)
    nssv186012634e-061270384
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