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nsv6875883

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:515,247

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2920 SVs from 94 studies. See in: genome view    
    Submitted genomic144,225,852-144,741,098Question Mark
    Overlapping variant regions from other studies: 2799 SVs from 94 studies. See in: genome view    
    Remapped(Score: Pass):145,280,755-145,966,483Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875883Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,225,852144,741,098
    nsv6875883RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,280,755145,966,483

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18737750duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18737750Submitted genomicNC_000008.11:g.144
    225852_144741098du
    p
    GRCh38 (hg38)NC_000008.11Chr8144,225,852144,741,098
    nssv18737750RemappedPassNC_000008.10:g.145
    280755_145966483du
    p
    GRCh37.p13First PassNC_000008.10Chr8145,280,755145,966,483

    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)
    nssv187377507e-062274368
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