A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788108



Internal ID19179207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31726528..32327926hg38UCSC Ensembl
Innerchr15:32018731..32620127hg19UCSC Ensembl
Innerchr15:29806023..30407419hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38601399
hg19601397
hg18601397
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892653
Supporting Variants
Samples
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=80
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788108
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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