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nsv6664841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:151

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 148 SVs from 28 studies. See in: genome view    
    Submitted genomic226,072,031-226,072,181Question Mark
    Overlapping variant regions from other studies: 151 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):226,259,732-226,259,882Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6664841Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1226,072,031226,072,181
    nsv6664841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1226,259,732226,259,882

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370351deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370351Submitted genomicNC_000001.11:g.226
    072031_226072181de
    l
    GRCh38 (hg38)NC_000001.11Chr1226,072,031226,072,181
    nssv18370351RemappedPerfectNC_000001.10:g.226
    259732_226259882de
    l
    GRCh37.p13First PassNC_000001.10Chr1226,259,732226,259,882

    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)
    nssv183703512.2e-056266682
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