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nsv6946625

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:399

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 34 studies. See in: genome view    
    Submitted genomic46,268,502-46,268,900Question Mark
    Overlapping variant regions from other studies: 150 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):46,842,637-46,843,035Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6946625Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1346,268,50246,268,900
    nsv6946625RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1346,842,63746,843,035

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18378163deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18378163Submitted genomicNC_000013.11:g.462
    68502_46268900del
    GRCh38 (hg38)NC_000013.11Chr1346,268,50246,268,900
    nssv18378163RemappedPerfectNC_000013.10:g.468
    42637_46843035del
    GRCh37.p13First PassNC_000013.10Chr1346,842,63746,843,035

    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)
    nssv183781630.0163919264772
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