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nsv6984145

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,057

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 20 studies. See in: genome view    
    Submitted genomic50,842,571-50,850,627Question Mark
    Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):48,919,932-48,927,988Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6984145Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1750,842,57150,850,627
    nsv6984145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1748,919,93248,927,988

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18411126deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18411126Submitted genomicNC_000017.11:g.508
    42571_50850627del
    GRCh38 (hg38)NC_000017.11Chr1750,842,57150,850,627
    nssv18411126RemappedPerfectNC_000017.10:g.489
    19932_48927988del
    GRCh37.p13First PassNC_000017.10Chr1748,919,93248,927,988

    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)
    nssv184111264e-061276262
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