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nsv6639503

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:646

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 19 studies. See in: genome view    
    Submitted genomic107,442,036-107,442,681Question Mark
    Overlapping variant regions from other studies: 125 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):107,984,658-107,985,303Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6639503Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1107,442,036107,442,681
    nsv6639503RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1107,984,658107,985,303

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586234duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586234Submitted genomicNC_000001.11:g.107
    442036_107442681du
    p
    GRCh38 (hg38)NC_000001.11Chr1107,442,036107,442,681
    nssv18586234RemappedPerfectNC_000001.10:g.107
    984658_107985303du
    p
    GRCh37.p13First PassNC_000001.10Chr1107,984,658107,985,303

    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)
    nssv185862344e-061248744
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