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nsv6972636

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,942

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 198 SVs from 37 studies. See in: genome view    
    Submitted genomic62,233,410-62,269,351Question Mark
    Overlapping variant regions from other studies: 198 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):62,525,609-62,561,550Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972636Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1562,233,41062,269,351
    nsv6972636RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1562,525,60962,561,550

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18395020deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18395020Submitted genomicNC_000015.10:g.622
    33410_62269351del
    GRCh38 (hg38)NC_000015.10Chr1562,233,41062,269,351
    nssv18395020RemappedPerfectNC_000015.9:g.6252
    5609_62561550del
    GRCh37.p13First PassNC_000015.9Chr1562,525,60962,561,550

    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)
    nssv183950204e-061276188
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