A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788938



Internal ID18816399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21048490..21235224hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg18186735
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892623
Supporting Variants
Samples
Known GenesGOLGA8S, LOC440243
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788938
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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