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nsv6346585

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:522,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1562 SVs from 84 studies. See in: genome view    
    Submitted genomic219,120,801-219,643,000Question Mark
    Overlapping variant regions from other studies: 1562 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):219,985,523-220,507,722Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6346585Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2219,120,801219,643,000
    nsv6346585RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2219,985,523220,507,722

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205638duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205638Submitted genomicNC_000002.12:g.219
    120801_219643000du
    p
    GRCh38 (hg38)NC_000002.12Chr2219,120,801219,643,000
    nssv18205638RemappedPerfectNC_000002.11:g.219
    985523_220507722du
    p
    GRCh37.p13First PassNC_000002.11Chr2219,985,523220,507,722

    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)
    nssv18205638<0.001128302
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