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nsv6990871

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:322,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 960 SVs from 75 studies. See in: genome view    
    Submitted genomic30,902,101-31,224,500Question Mark
    Overlapping variant regions from other studies: 960 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):30,913,422-31,235,821Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1630,902,10131,224,500
    nsv6990871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1630,913,42231,235,821

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18622370duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18622370Submitted genomicNC_000016.10:g.309
    02101_31224500dup
    GRCh38 (hg38)NC_000016.10Chr1630,902,10131,224,500
    nssv18622370RemappedPerfectNC_000016.9:g.3091
    3422_31235821dup
    GRCh37.p13First PassNC_000016.9Chr1630,913,42231,235,821

    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)
    nssv186223701.5e-054267066
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