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nsv6865860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,232

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 954 SVs from 76 studies. See in: genome view    
    Submitted genomic143,536,657-143,611,888Question Mark
    Overlapping variant regions from other studies: 954 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):144,618,827-144,694,058Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6865860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8143,536,657143,611,888
    nsv6865860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8144,618,827144,694,058

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738659duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738659Submitted genomicNC_000008.11:g.143
    536657_143611888du
    p
    GRCh38 (hg38)NC_000008.11Chr8143,536,657143,611,888
    nssv18738659RemappedPerfectNC_000008.10:g.144
    618827_144694058du
    p
    GRCh37.p13First PassNC_000008.10Chr8144,618,827144,694,058

    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)
    nssv187386594e-061275866
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