A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893671



Internal ID18837805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21918975..22242630hg38UCSC Ensembl
Outerchr3:21918975..22242630hg38UCSC Ensembl
Innerchr3:21960467..22284122hg19UCSC Ensembl
Outerchr3:21960467..22284122hg19UCSC Ensembl
Innerchr3:21935471..22259126hg18UCSC Ensembl
Outerchr3:21935471..22259126hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38323656
hg19323656
hg18323656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796231
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893671
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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