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nsv7070234

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 22 studies. See in: genome view    
    Submitted genomic101,670,169-101,670,185Question Mark
    Overlapping variant regions from other studies: 114 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):103,429,926-103,429,942Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070234Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10101,670,169101,670,185
    nsv7070234RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,429,926103,429,942

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744099inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744099Submitted genomicNC_000010.11:g.101
    670169_101670185in
    v
    GRCh38 (hg38)NC_000010.11Chr10101,670,169101,670,185
    nssv18744099RemappedPerfectNC_000010.10:g.103
    429926_103429942in
    v
    GRCh37.p13First PassNC_000010.10Chr10103,429,926103,429,942

    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)
    nssv187440994e-061276262
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