A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4191n54



Internal ID22772086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20367552..20442400hg38UCSC Ensembl
chr15:20572805..20647653hg19UCSC Ensembl
chr15:18832819..18907667hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3874849
hg1974849
hg1874849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567348, nsv567349
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4191n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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