A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668290



Internal ID9934395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27654385..27656541hg38UCSC Ensembl
Outerchr3:27654228..27656694hg38UCSC Ensembl
Innerchr3:27695876..27698032hg19UCSC Ensembl
Outerchr3:27695719..27698185hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg382467
hg192467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6119996
SamplesNA18964
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668290
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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