A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25795994



Internal ID18813527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34515650hg38UCSC Ensembl
Innerchr15:34718594..34807851hg19UCSC Ensembl
Innerchr15:32505886..32595143hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3889258
hg1989258
hg1889258
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892663
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25795994
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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