A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9174n54



Internal ID19001350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94757862..94758645hg38UCSC Ensembl
chr4:95679013..95679796hg19UCSC Ensembl
chr4:95898036..95898819hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38784
hg19784
hg18784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594903, nsv594904, nsv594902
Samples
Known GenesBMPR1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9174n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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