A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3922n54



Internal ID22771817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101702580..101727209hg38UCSC Ensembl
chr14:102168917..102193546hg19UCSC Ensembl
chr14:101238670..101263299hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3824630
hg1924630
hg1824630
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565897, nsv565888
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3922n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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