A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3996n54



Internal ID22771891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105474226..105488519hg38UCSC Ensembl
chr14:105940563..105954856hg19UCSC Ensembl
chr14:105011608..105025901hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3814294
hg1914294
hg1814294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566256, nsv566237, nsv566250
Samples
Known GenesCRIP1, CRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3996n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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