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nsv7043618

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:382,258

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1679 SVs from 95 studies. See in: genome view    
    Submitted genomic140,515,390-140,897,647Question Mark
    Overlapping variant regions from other studies: 658 SVs from 63 studies. See in: genome view    
    Remapped(Score: Pass):139,894,975-140,144,409Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043618Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5140,515,390140,897,647
    nsv7043618RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5139,894,975140,144,409

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774488inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774488Submitted genomicNC_000005.10:g.140
    515390_140897647in
    v
    GRCh38 (hg38)NC_000005.10Chr5140,515,390140,897,647
    nssv18774488RemappedPassNC_000005.9:g.1398
    94975_140144409inv
    GRCh37.p13First PassNC_000005.9Chr5139,894,975140,144,409

    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)
    nssv187744882.5e-057274062
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