A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4198n54



Internal ID22772093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20376987..20420298hg38UCSC Ensembl
chr15:20582240..20625551hg19UCSC Ensembl
chr15:18842254..18885565hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3843312
hg1943312
hg1843312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv567407, nsv567431, nsv567436, nsv567444, nsv567449, nsv567427, nsv567387, nsv567377, nsv567445, nsv567434, nsv567376, nsv567378, nsv567388, nsv567435, nsv567399, nsv567439, nsv567433, nsv567420, nsv567401, nsv567440, nsv567400
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4198n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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