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nsv7048291

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:395,006

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2195 SVs from 107 studies. See in: genome view    
    Submitted genomic12,842,405-13,237,410Question Mark
    Overlapping variant regions from other studies: 2619 SVs from 108 studies. See in: genome view    
    Remapped(Score: Pass):12,902,258-13,468,432Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048291Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr112,842,40513,237,410
    nsv7048291RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr112,902,25813,468,432

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18745993inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18745993Submitted genomicNC_000001.11:g.128
    42405_13237410inv
    GRCh38 (hg38)NC_000001.11Chr112,842,40513,237,410
    nssv18745993RemappedPassNC_000001.10:g.129
    02258_13468432inv
    GRCh37.p13First PassNC_000001.10Chr112,902,25813,468,432

    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)
    nssv18745993<0.00160274456
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