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nsv6693819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 163 SVs from 26 studies. See in: genome view    
    Submitted genomic169,477,201-169,480,000Question Mark
    Overlapping variant regions from other studies: 163 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):170,333,711-170,336,510Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6693819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,477,201169,480,000
    nsv6693819RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2170,333,711170,336,510

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18444317deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18444317Submitted genomicNC_000002.12:g.169
    477201_169480000de
    l
    GRCh38 (hg38)NC_000002.12Chr2169,477,201169,480,000
    nssv18444317RemappedPerfectNC_000002.11:g.170
    333711_170336510de
    l
    GRCh37.p13First PassNC_000002.11Chr2170,333,711170,336,510

    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)
    nssv184443171.1e-052275628
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