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nsv7003742

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,880

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 252 SVs from 41 studies. See in: genome view    
    Submitted genomic1,442,340-1,448,219Question Mark
    Overlapping variant regions from other studies: 252 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):1,442,339-1,448,218Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7003742Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr191,442,3401,448,219
    nsv7003742RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr191,442,3391,448,218

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18636545duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18636545Submitted genomicNC_000019.10:g.144
    2340_1448219dup
    GRCh38 (hg38)NC_000019.10Chr191,442,3401,448,219
    nssv18636545RemappedPerfectNC_000019.9:g.1442
    339_1448218dup
    GRCh37.p13First PassNC_000019.9Chr191,442,3391,448,218

    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)
    nssv186365454e-061272612
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