A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791976



Internal ID18829415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23333216..23517201hg38UCSC Ensembl
Innerchr15:23578363..23762348hg19UCSC Ensembl
Innerchr15:21129804..21313441hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38183986
hg19183986
hg18183638
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=38
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791976
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer