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nsv7044547

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,037,518

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17144 SVs from 123 studies. See in: genome view    
    Submitted genomic234,053,817-240,091,334Question Mark
    Overlapping variant regions from other studies: 17134 SVs from 123 studies. See in: genome view    
    Remapped(Score: Good):234,189,563-240,254,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044547Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1234,053,817240,091,334
    nsv7044547RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1234,189,563240,254,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758688inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758688Submitted genomicNC_000001.11:g.234
    053817_240091334in
    v
    GRCh38 (hg38)NC_000001.11Chr1234,053,817240,091,334
    nssv18758688RemappedGoodNC_000001.10:g.234
    189563_240254634in
    v
    GRCh37.p13First PassNC_000001.10Chr1234,189,563240,254,634

    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)
    nssv187586881.1e-053274840
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