A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5246n54



Internal ID22773141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81035591..81036505hg38UCSC Ensembl
chr16:81069196..81070110hg19UCSC Ensembl
chr16:79626697..79627611hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38915
hg19915
hg18915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573341, nsv573342, nsv573340, nsv573339
Samples
Known GenesATMIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5246n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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