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nsv6950541

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 26 studies. See in: genome view    
    Submitted genomic53,936,601-53,968,700Question Mark
    Overlapping variant regions from other studies: 144 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):54,403,319-54,435,418Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6950541Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1453,936,60153,968,700
    nsv6950541RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1454,403,31954,435,418

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18616285duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18616285Submitted genomicNC_000014.9:g.5393
    6601_53968700dup
    GRCh38 (hg38)NC_000014.9Chr1453,936,60153,968,700
    nssv18616285RemappedPerfectNC_000014.8:g.5440
    3319_54435418dup
    GRCh37.p13First PassNC_000014.8Chr1454,403,31954,435,418

    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)
    nssv186162854e-061272776
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