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nsv7074464

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,869,984

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 21971 SVs from 117 studies. See in: genome view    
    Submitted genomic43,918,591-49,788,574Question Mark
    Overlapping variant regions from other studies: 21925 SVs from 117 studies. See in: genome view    
    Remapped(Score: Good):44,314,471-50,182,222Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074464Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2243,918,59149,788,574
    nsv7074464RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2244,314,47150,182,222

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762720inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762720Submitted genomicNC_000022.11:g.439
    18591_49788574inv
    GRCh38 (hg38)NC_000022.11Chr2243,918,59149,788,574
    nssv18762720RemappedGoodNC_000022.10:g.443
    14471_50182222inv
    GRCh37.p13First PassNC_000022.10Chr2244,314,47150,182,222

    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)
    nssv187627204e-061276268
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