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nsv6462201

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:329,460

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 941 SVs from 70 studies. See in: genome view    
    Submitted genomic52,520,433-52,849,892Question Mark
    Overlapping variant regions from other studies: 941 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):52,914,217-53,243,676Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6462201Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,520,43352,849,892
    nsv6462201RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,914,21753,243,676

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18188293duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18188293Submitted genomicNC_000012.12:g.525
    20433_52849892dup
    GRCh38 (hg38)NC_000012.12Chr1252,520,43352,849,892
    nssv18188293RemappedPerfectNC_000012.11:g.529
    14217_53243676dup
    GRCh37.p13First PassNC_000012.11Chr1252,914,21753,243,676

    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)
    nssv18188293<0.001139266
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