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nsv6926874

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,236

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 81 SVs from 24 studies. See in: genome view    
    Submitted genomic39,382,840-39,384,075Question Mark
    Overlapping variant regions from other studies: 81 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):39,776,642-39,777,877Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6926874Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1239,382,84039,384,075
    nsv6926874RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1239,776,64239,777,877

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18597498duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18597498Submitted genomicNC_000012.12:g.393
    82840_39384075dup
    GRCh38 (hg38)NC_000012.12Chr1239,382,84039,384,075
    nssv18597498RemappedPerfectNC_000012.11:g.397
    76642_39777877dup
    GRCh37.p13First PassNC_000012.11Chr1239,776,64239,777,877

    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)
    nssv185974984e-061265142
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