A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4208n54



Internal ID22772103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20399391..20421580hg38UCSC Ensembl
chr15:20604644..20626833hg19UCSC Ensembl
chr15:18864658..18886847hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3822190
hg1922190
hg1822190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567457, nsv567460, nsv567462, nsv567463
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4208n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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