A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797901



Internal ID18827125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35227916..35233861hg38UCSC Ensembl
Innerchr19:35718819..35724764hg19UCSC Ensembl
Innerchr19:40410659..40416604hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385946
hg195946
hg185946
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893200
Supporting Variants
Samples
Known GenesFAM187B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797901
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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