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nsv6684214

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 197 SVs from 48 studies. See in: genome view    
    Submitted genomic88,042,001-88,079,900Question Mark
    Overlapping variant regions from other studies: 199 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):88,341,520-88,379,419Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6684214Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr288,042,00188,079,900
    nsv6684214RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr288,341,52088,379,419

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18669072duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18669072Submitted genomicNC_000002.12:g.880
    42001_88079900dup
    GRCh38 (hg38)NC_000002.12Chr288,042,00188,079,900
    nssv18669072RemappedPerfectNC_000002.11:g.883
    41520_88379419dup
    GRCh37.p13First PassNC_000002.11Chr288,341,52088,379,419

    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)
    nssv186690724e-061274744
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