nsv6558782

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,027,197

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11015 SVs from 118 studies. See in: genome view    
    Submitted genomic143,001,224-145,028,420Question Mark
    Overlapping variant regions from other studies: 10723 SVs from 118 studies. See in: genome view    
    Remapped(Score: Pass):144,082,641-146,253,806Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6558782Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8143,001,224145,028,420
    nsv6558782RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8144,082,641146,253,806

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18277297inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18277297Submitted genomicNC_000008.11:g.143
    001224_145028420in
    v
    GRCh38 (hg38)NC_000008.11Chr8143,001,224145,028,420
    nssv18277297RemappedPassNC_000008.10:g.144
    082641_146253806in
    v
    GRCh37.p13First PassNC_000008.10Chr8144,082,641146,253,806

    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)
    nssv18277297<0.001139304
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