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nsv7070460

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,098,121

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 18191 SVs from 128 studies. See in: genome view    
    Submitted genomic21,520,035-27,618,155Question Mark
    Overlapping variant regions from other studies: 18193 SVs from 128 studies. See in: genome view    
    Remapped(Score: Perfect):21,541,581-27,639,702Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070460Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1121,520,03527,618,155
    nsv7070460RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1121,541,58127,639,702

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739371inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739371Submitted genomicNC_000011.10:g.215
    20035_27618155inv
    GRCh38 (hg38)NC_000011.10Chr1121,520,03527,618,155
    nssv18739371RemappedPerfectNC_000011.9:g.2154
    1581_27639702inv
    GRCh37.p13First PassNC_000011.9Chr1121,541,58127,639,702

    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)
    nssv187393714e-061276268
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