U.S. flag

An official website of the United States government

nsv7028071

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 203 SVs from 43 studies. See in: genome view    
    Submitted genomic34,200,901-34,214,700Question Mark
    Overlapping variant regions from other studies: 203 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):32,788,707-32,802,506Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028071Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2034,200,90134,214,700
    nsv7028071RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2032,788,70732,802,506

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642041duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642041Submitted genomicNC_000020.11:g.342
    00901_34214700dup
    GRCh38 (hg38)NC_000020.11Chr2034,200,90134,214,700
    nssv18642041RemappedPerfectNC_000020.10:g.327
    88707_32802506dup
    GRCh37.p13First PassNC_000020.10Chr2032,788,70732,802,506

    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)
    nssv186420414e-061275914
    Support Center