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nsv7042984

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,931,771

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13741 SVs from 121 studies. See in: genome view    
    Submitted genomic26,886,657-32,818,427Question Mark
    Overlapping variant regions from other studies: 13758 SVs from 122 studies. See in: genome view    
    Remapped(Score: Good):27,109,525-33,043,494Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042984Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr226,886,65732,818,427
    nsv7042984RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr227,109,52533,043,494

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18768755inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18768755Submitted genomicNC_000002.12:g.268
    86657_32818427inv
    GRCh38 (hg38)NC_000002.12Chr226,886,65732,818,427
    nssv18768755RemappedGoodNC_000002.11:g.271
    09525_33043494inv
    GRCh37.p13First PassNC_000002.11Chr227,109,52533,043,494

    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)
    nssv187687554e-061276268
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