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nsv6556844

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,732,980

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15441 SVs from 123 studies. See in: genome view    
    Submitted genomic161,649,493-166,382,472Question Mark
    Overlapping variant regions from other studies: 15432 SVs from 123 studies. See in: genome view    
    Remapped(Score: Good):162,070,525-166,795,960Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6556844Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6161,649,493166,382,472
    nsv6556844RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6162,070,525166,795,960

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18269873inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18269873Submitted genomicNC_000006.12:g.161
    649493_166382472in
    v
    GRCh38 (hg38)NC_000006.12Chr6161,649,493166,382,472
    nssv18269873RemappedGoodNC_000006.11:g.162
    070525_166795960in
    v
    GRCh37.p13First PassNC_000006.11Chr6162,070,525166,795,960

    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)
    nssv18269873<0.001139304
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