A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798083



Internal ID19159638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15543065..15551953hg38UCSC Ensembl
Innerchr8:15400574..15409462hg19UCSC Ensembl
Innerchr8:15444945..15453833hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388889
hg198889
hg188889
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891350
Supporting Variants
Samples
Known GenesTUSC3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798083
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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