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nsv6563487

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:497

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 203 SVs from 19 studies. See in: genome view    
    Submitted genomic123,268,009-123,268,505Question Mark
    Overlapping variant regions from other studies: 203 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):124,280,249-124,280,745Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6563487Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8123,268,009123,268,505
    nsv6563487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8124,280,249124,280,745

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18276110inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18276110Submitted genomicNC_000008.11:g.123
    268009_123268505in
    v
    GRCh38 (hg38)NC_000008.11Chr8123,268,009123,268,505
    nssv18276110RemappedPerfectNC_000008.10:g.124
    280249_124280745in
    v
    GRCh37.p13First PassNC_000008.10Chr8124,280,249124,280,745

    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)
    nssv18276110<0.001534710
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