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nsv7063478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:181,743

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 828 SVs from 75 studies. See in: genome view    
    Submitted genomic46,955,918-47,137,660Question Mark
    Overlapping variant regions from other studies: 811 SVs from 75 studies. See in: genome view    
    Remapped(Score: Good):47,351,814-47,533,303Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2246,955,91847,137,660
    nsv7063478RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2247,351,81447,533,303

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18763569inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18763569Submitted genomicNC_000022.11:g.469
    55918_47137660inv
    GRCh38 (hg38)NC_000022.11Chr2246,955,91847,137,660
    nssv18763569RemappedGoodNC_000022.10:g.473
    51814_47533303inv
    GRCh37.p13First PassNC_000022.10Chr2247,351,81447,533,303

    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)
    nssv187635694e-061276268
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