A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3994n54



Internal ID22771889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105474172..105477662hg38UCSC Ensembl
chr14:105940509..105943999hg19UCSC Ensembl
chr14:105011554..105015044hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg383491
hg193491
hg183491
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566264, nsv566262, nsv566247, nsv566228, nsv566243
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3994n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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