A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787681



Internal ID18824208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34508394hg38UCSC Ensembl
Innerchr15:34718594..34800595hg19UCSC Ensembl
Innerchr15:32505886..32587887hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3882002
hg1982002
hg1882002
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 HumanHap 550
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787681
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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