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nsv6875113

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:813

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 196 SVs from 45 studies. See in: genome view    
    Submitted genomic144,831,651-144,832,463Question Mark
    Overlapping variant regions from other studies: 196 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):146,057,036-146,057,848Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875113Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,831,651144,832,463
    nsv6875113RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8146,057,036146,057,848

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18553312deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18553312Submitted genomicNC_000008.11:g.144
    831651_144832463de
    l
    GRCh38 (hg38)NC_000008.11Chr8144,831,651144,832,463
    nssv18553312RemappedPerfectNC_000008.10:g.146
    057036_146057848de
    l
    GRCh37.p13First PassNC_000008.10Chr8146,057,036146,057,848

    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)
    nssv185533120.511139709272520
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