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nsv6545914

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 170 SVs from 30 studies. See in: genome view    
    Submitted genomic33,541,301-33,549,400Question Mark
    Overlapping variant regions from other studies: 170 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):34,913,607-34,921,706Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6545914Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2133,541,30133,549,400
    nsv6545914RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2134,913,60734,921,706

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18203916duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18203916Submitted genomicNC_000021.9:g.3354
    1301_33549400dup
    GRCh38 (hg38)NC_000021.9Chr2133,541,30133,549,400
    nssv18203916RemappedPerfectNC_000021.8:g.3491
    3607_34921706dup
    GRCh37.p13First PassNC_000021.8Chr2134,913,60734,921,706

    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)
    nssv18203916<0.001239178
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