A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4184n54



Internal ID22772079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20334643..20428007hg38UCSC Ensembl
chr15:20539896..20633260hg19UCSC Ensembl
chr15:18799910..18893274hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3893365
hg1993365
hg1893365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567326, nsv567335, nsv567334, nsv567324, nsv567336, nsv567333, nsv567337
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4184n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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