A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796234



Internal ID19159550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4093768..4195663hg38UCSC Ensembl
Innerchr3:4135452..4237347hg19UCSC Ensembl
Innerchr3:4110452..4212347hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38101896
hg19101896
hg18101896
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893628
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796234
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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