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nsv6866250

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:790,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4029 SVs from 98 studies. See in: genome view    
    Submitted genomic143,771,901-144,562,100Question Mark
    Overlapping variant regions from other studies: 2614 SVs from 91 studies. See in: genome view    
    Remapped(Score: Pass):145,146,063-145,787,484Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6866250Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8143,771,901144,562,100
    nsv6866250RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,146,063145,787,484

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731395duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731395Submitted genomicNC_000008.11:g.143
    771901_144562100du
    p
    GRCh38 (hg38)NC_000008.11Chr8143,771,901144,562,100
    nssv18731395RemappedPassNC_000008.10:g.145
    146063_145787484du
    p
    GRCh37.p13First PassNC_000008.10Chr8145,146,063145,787,484

    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)
    nssv187313954e-061273846
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