A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893191



Internal ID19184011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27287920..27669006hg38UCSC Ensembl
Outerchr19:27272532..27767872hg38UCSC Ensembl
Innerchr19:27778828..28159914hg19UCSC Ensembl
Outerchr19:27763440..28258780hg19UCSC Ensembl
Innerchr19:32470668..32851754hg18UCSC Ensembl
Outerchr19:32455280..32950620hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38495341
hg19495341
hg18495341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792523, essv25790145, essv25788464
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893191
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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