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nsv6351412

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,001

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 19 studies. See in: genome view    
    Submitted genomic168,778,410-168,785,410Question Mark
    Overlapping variant regions from other studies: 127 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):169,634,920-169,641,920Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6351412Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2168,778,410168,785,410
    nsv6351412RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2169,634,920169,641,920

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18079930deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18079930Submitted genomicNC_000002.12:g.168
    778410_168785410de
    l
    GRCh38 (hg38)NC_000002.12Chr2168,778,410168,785,410
    nssv18079930RemappedPerfectNC_000002.11:g.169
    634920_169641920de
    l
    GRCh37.p13First PassNC_000002.11Chr2169,634,920169,641,920

    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)
    nssv18079930<0.001139212
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