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nsv7052780

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:108

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 19 studies. See in: genome view    
    Submitted genomic150,724,949-150,725,056Question Mark
    Overlapping variant regions from other studies: 92 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):151,046,085-151,046,192Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052780Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6150,724,949150,725,056
    nsv7052780RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6151,046,085151,046,192

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18779110inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18779110Submitted genomicNC_000006.12:g.150
    724949_150725056in
    v
    GRCh38 (hg38)NC_000006.12Chr6150,724,949150,725,056
    nssv18779110RemappedPerfectNC_000006.11:g.151
    046085_151046192in
    v
    GRCh37.p13First PassNC_000006.11Chr6151,046,085151,046,192

    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)
    nssv187791104e-061276268
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