A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3761n54



Internal ID20137185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73527984..73561413hg38UCSC Ensembl
chr14:73994688..74028117hg19UCSC Ensembl
chr14:73064441..73097870hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3833430
hg1933430
hg1833430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565114, nsv565113, nsv565112
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3761n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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