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nsv6431945

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 208 SVs from 20 studies. See in: genome view    
    Submitted genomic123,248,101-123,250,000Question Mark
    Overlapping variant regions from other studies: 208 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):124,260,341-124,262,240Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6431945Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8123,248,101123,250,000
    nsv6431945RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8124,260,341124,262,240

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18164006deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18164006Submitted genomicNC_000008.11:g.123
    248101_123250000de
    l
    GRCh38 (hg38)NC_000008.11Chr8123,248,101123,250,000
    nssv18164006RemappedPerfectNC_000008.10:g.124
    260341_124262240de
    l
    GRCh37.p13First PassNC_000008.10Chr8124,260,341124,262,240

    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)
    nssv18164006<0.001539064
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