A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788854



Internal ID18820816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2489783..2878245hg38UCSC Ensembl
Innerchr8:2346899..2735767hg19UCSC Ensembl
Innerchr8:2334306..2723174hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38388463
hg19388869
hg18388869
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891260
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=135
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788854
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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