A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4207n54



Internal ID22772102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20389712..20420026hg38UCSC Ensembl
chr15:20594965..20625279hg19UCSC Ensembl
chr15:18854979..18885293hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3830315
hg1930315
hg1830315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567452, nsv567455, nsv567453, nsv567454, nsv567456
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4207n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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