U.S. flag

An official website of the United States government

nsv6962873

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,612

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 257 SVs from 43 studies. See in: genome view    
    Submitted genomic62,210,007-62,267,618Question Mark
    Overlapping variant regions from other studies: 257 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):62,502,206-62,559,817Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962873Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1562,210,00762,267,618
    nsv6962873RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1562,502,20662,559,817

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18395018deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18395018Submitted genomicNC_000015.10:g.622
    10007_62267618del
    GRCh38 (hg38)NC_000015.10Chr1562,210,00762,267,618
    nssv18395018RemappedPerfectNC_000015.9:g.6250
    2206_62559817del
    GRCh37.p13First PassNC_000015.9Chr1562,502,20662,559,817

    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)
    nssv183950181.4e-054276142
    Support Center