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nsv7040531

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,035,263

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9050 SVs from 110 studies. See in: genome view    
    Submitted genomic151,482,879-155,518,141Question Mark
    Overlapping variant regions from other studies: 9050 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):150,862,440-154,897,701Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040531Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5151,482,879155,518,141
    nsv7040531RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5150,862,440154,897,701

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774324inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774324Submitted genomicNC_000005.10:g.151
    482879_155518141in
    v
    GRCh38 (hg38)NC_000005.10Chr5151,482,879155,518,141
    nssv18774324RemappedPerfectNC_000005.9:g.1508
    62440_154897701inv
    GRCh37.p13First PassNC_000005.9Chr5150,862,440154,897,701

    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)
    nssv187743244e-061276268
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