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nsv7054232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,959

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 194 SVs from 38 studies. See in: genome view    
    Submitted genomic151,531,808-151,557,766Question Mark
    Overlapping variant regions from other studies: 194 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):151,852,943-151,878,901Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6151,531,808151,557,766
    nsv7054232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6151,852,943151,878,901

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18779116inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18779116Submitted genomicNC_000006.12:g.151
    531808_151557766in
    v
    GRCh38 (hg38)NC_000006.12Chr6151,531,808151,557,766
    nssv18779116RemappedPerfectNC_000006.11:g.151
    852943_151878901in
    v
    GRCh37.p13First PassNC_000006.11Chr6151,852,943151,878,901

    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)
    nssv187791164e-061276268
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