U.S. flag

An official website of the United States government

nsv6696585

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,561

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 170 SVs from 33 studies. See in: genome view    
    Submitted genomic202,398,866-202,405,426Question Mark
    Overlapping variant regions from other studies: 170 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):203,263,589-203,270,149Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6696585Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2202,398,866202,405,426
    nsv6696585RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2203,263,589203,270,149

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18659664duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18659664Submitted genomicNC_000002.12:g.202
    398866_202405426du
    p
    GRCh38 (hg38)NC_000002.12Chr2202,398,866202,405,426
    nssv18659664RemappedPerfectNC_000002.11:g.203
    263589_203270149du
    p
    GRCh37.p13First PassNC_000002.11Chr2203,263,589203,270,149

    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)
    nssv18659664<0.00144274070
    Support Center