A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8884n54



Internal ID20142308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1086603..1087362hg38UCSC Ensembl
chr4:1080391..1081150hg19UCSC Ensembl
chr4:1070391..1071150hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38760
hg19760
hg18760
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593246, nsv593252, nsv593253
Samples
Known GenesRNF212
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8884n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss5
Observed Complex0
Frequencyn/a


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