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nsv7043344

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:260,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1022 SVs from 67 studies. See in: genome view    
    Submitted genomic245,132,617-245,393,116Question Mark
    Overlapping variant regions from other studies: 1025 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):245,295,919-245,556,418Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043344Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,132,617245,393,116
    nsv7043344RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,295,919245,556,418

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759461inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759461Submitted genomicNC_000001.11:g.245
    132617_245393116in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,132,617245,393,116
    nssv18759461RemappedPerfectNC_000001.10:g.245
    295919_245556418in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,295,919245,556,418

    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)
    nssv187594617e-062273856
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