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nsv6877863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:490

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 235 SVs from 42 studies. See in: genome view    
    Submitted genomic142,316,691-142,317,180Question Mark
    Overlapping variant regions from other studies: 235 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):143,398,052-143,398,541Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6877863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8142,316,691142,317,180
    nsv6877863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8143,398,052143,398,541

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18551758deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18551758Submitted genomicNC_000008.11:g.142
    316691_142317180de
    l
    GRCh38 (hg38)NC_000008.11Chr8142,316,691142,317,180
    nssv18551758RemappedPerfectNC_000008.10:g.143
    398052_143398541de
    l
    GRCh37.p13First PassNC_000008.10Chr8143,398,052143,398,541

    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)
    nssv185517580.0061520243944
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