U.S. flag

An official website of the United States government

nsv6962303

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:555,061

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3251 SVs from 102 studies. See in: genome view    
    Submitted genomic1,118,142-1,673,202Question Mark
    Overlapping variant regions from other studies: 3251 SVs from 102 studies. See in: genome view    
    Remapped(Score: Perfect):1,168,142-1,723,203Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,118,1421,673,202
    nsv6962303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,168,1421,723,203

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18620537duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18620537Submitted genomicNC_000016.10:g.111
    8142_1673202dup
    GRCh38 (hg38)NC_000016.10Chr161,118,1421,673,202
    nssv18620537RemappedPerfectNC_000016.9:g.1168
    142_1723203dup
    GRCh37.p13First PassNC_000016.9Chr161,168,1421,723,203

    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)
    nssv186205374e-061275478
    Support Center