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nsv6688920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:335

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 33 studies. See in: genome view    
    Submitted genomic169,484,989-169,485,323Question Mark
    Overlapping variant regions from other studies: 193 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):170,341,499-170,341,833Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6688920Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,484,989169,485,323
    nsv6688920RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2170,341,499170,341,833

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18650527duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18650527Submitted genomicNC_000002.12:g.169
    484989_169485323du
    p
    GRCh38 (hg38)NC_000002.12Chr2169,484,989169,485,323
    nssv18650527RemappedPerfectNC_000002.11:g.170
    341499_170341833du
    p
    GRCh37.p13First PassNC_000002.11Chr2170,341,499170,341,833

    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)
    nssv186505270.08820808234658
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