A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984482



Internal ID12977058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23989660..24226860hg38UCSC Ensembl
Innerchr15:24234807..24472007hg19UCSC Ensembl
Innerchr15:21785900..22023100hg18UCSC Ensembl
Innerchr15:21785900..22023100hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38237201
hg19237201
hg18237201
hg17237201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751512
Supporting Variants
SamplesBEC_711
Known GenesPWRN2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984482
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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