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nsv6802471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:145

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
    Submitted genomic87,679,193-87,679,337Question Mark
    Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):88,388,911-88,389,055Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6802471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr687,679,19387,679,337
    nsv6802471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr688,388,91188,389,055

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18719992duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18719992Submitted genomicNC_000006.12:g.876
    79193_87679337dup
    GRCh38 (hg38)NC_000006.12Chr687,679,19387,679,337
    nssv18719992RemappedPerfectNC_000006.11:g.883
    88911_88389055dup
    GRCh37.p13First PassNC_000006.11Chr688,388,91188,389,055

    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)
    nssv187199920.0327032223208
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