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nsv6858066

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:358,208

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 981 SVs from 63 studies. See in: genome view    
    Submitted genomic73,912,974-74,271,181Question Mark
    Overlapping variant regions from other studies: 981 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):74,825,209-75,183,416Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6858066Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr873,912,97474,271,181
    nsv6858066RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr874,825,20975,183,416

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739796duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739796Submitted genomicNC_000008.11:g.739
    12974_74271181dup
    GRCh38 (hg38)NC_000008.11Chr873,912,97474,271,181
    nssv18739796RemappedPerfectNC_000008.10:g.748
    25209_75183416dup
    GRCh37.p13First PassNC_000008.10Chr874,825,20975,183,416

    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)
    nssv187397964e-061275102
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