U.S. flag

An official website of the United States government

nsv7020043

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49,270

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 237 SVs from 41 studies. See in: genome view    
    Submitted genomic45,169,630-45,218,899Question Mark
    Overlapping variant regions from other studies: 237 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):43,798,271-43,847,540Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7020043Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2045,169,63045,218,899
    nsv7020043RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,798,27143,847,540

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642206duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642206Submitted genomicNC_000020.11:g.451
    69630_45218899dup
    GRCh38 (hg38)NC_000020.11Chr2045,169,63045,218,899
    nssv18642206RemappedPerfectNC_000020.10:g.437
    98271_43847540dup
    GRCh37.p13First PassNC_000020.10Chr2043,798,27143,847,540

    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)
    nssv186422067e-062275320
    Support Center