A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797350



Internal ID19181117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9181086..9309665hg38UCSC Ensembl
Innerchr8:9038596..9167175hg19UCSC Ensembl
Innerchr8:9076006..9204585hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38128580
hg19128580
hg18128580
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891330
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=55
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797350
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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