A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3989n54



Internal ID20137413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105468704..105475240hg38UCSC Ensembl
chr14:105935041..105941577hg19UCSC Ensembl
chr14:105006086..105012622hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg386537
hg196537
hg186537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566215, nsv566213
Samples
Known GenesCRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3989n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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