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nsv6646901

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 163 SVs from 36 studies. See in: genome view    
    Submitted genomic19,781,001-19,812,500Question Mark
    Overlapping variant regions from other studies: 163 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):20,107,494-20,138,993Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6646901Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,781,00119,812,500
    nsv6646901RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr120,107,49420,138,993

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18607135duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18607135Submitted genomicNC_000001.11:g.197
    81001_19812500dup
    GRCh38 (hg38)NC_000001.11Chr119,781,00119,812,500
    nssv18607135RemappedPerfectNC_000001.10:g.201
    07494_20138993dup
    GRCh37.p13First PassNC_000001.10Chr120,107,49420,138,993

    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)
    nssv186071353.2e-059273058
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