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nsv6868929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,235

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 534 SVs from 62 studies. See in: genome view    
    Submitted genomic144,423,852-144,451,086Question Mark
    Overlapping variant regions from other studies: 509 SVs from 60 studies. See in: genome view    
    Remapped(Score: Pass):145,659,902-145,676,469Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6868929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,423,852144,451,086
    nsv6868929RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,659,902145,676,469

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18733336duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18733336Submitted genomicNC_000008.11:g.144
    423852_144451086du
    p
    GRCh38 (hg38)NC_000008.11Chr8144,423,852144,451,086
    nssv18733336RemappedPassNC_000008.10:g.145
    659902_145676469du
    p
    GRCh37.p13First PassNC_000008.10Chr8145,659,902145,676,469

    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)
    nssv187333364e-061276004
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