A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790145



Internal ID19170756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27272532..27767872hg38UCSC Ensembl
Innerchr19:27763440..28258780hg19UCSC Ensembl
Innerchr19:32455280..32950620hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38495341
hg19495341
hg18495341
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893191
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=55
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790145
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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