A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893200



Internal ID18837334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35227916..35233861hg38UCSC Ensembl
Outerchr19:35227916..35233861hg38UCSC Ensembl
Innerchr19:35718819..35724764hg19UCSC Ensembl
Outerchr19:35718819..35724764hg19UCSC Ensembl
Innerchr19:40410659..40416604hg18UCSC Ensembl
Outerchr19:40410659..40416604hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385946
hg195946
hg185946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797901
Samples
Known GenesFAM187B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893200
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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