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nsv7061071

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:206,030

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 582 SVs from 67 studies. See in: genome view    
    Submitted genomic64,416,765-64,622,794Question Mark
    Overlapping variant regions from other studies: 582 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):64,184,237-64,390,266Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061071Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1164,416,76564,622,794
    nsv7061071RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1164,184,23764,390,266

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744474inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744474Submitted genomicNC_000011.10:g.644
    16765_64622794inv
    GRCh38 (hg38)NC_000011.10Chr1164,416,76564,622,794
    nssv18744474RemappedPerfectNC_000011.9:g.6418
    4237_64390266inv
    GRCh37.p13First PassNC_000011.9Chr1164,184,23764,390,266

    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)
    nssv187444744e-061276268
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