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nsv7052273

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,357,782

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 19708 SVs from 125 studies. See in: genome view    
    Submitted genomic153,428,141-160,785,922Question Mark
    Overlapping variant regions from other studies: 19710 SVs from 125 studies. See in: genome view    
    Remapped(Score: Good):153,749,276-161,206,954Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052273Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6153,428,141160,785,922
    nsv7052273RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6153,749,276161,206,954

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18779144inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18779144Submitted genomicNC_000006.12:g.153
    428141_160785922in
    v
    GRCh38 (hg38)NC_000006.12Chr6153,428,141160,785,922
    nssv18779144RemappedGoodNC_000006.11:g.153
    749276_161206954in
    v
    GRCh37.p13First PassNC_000006.11Chr6153,749,276161,206,954

    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)
    nssv187791440.39399411253050
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