A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665969



Internal ID9932074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33668156..33679203hg38UCSC Ensembl
chr4:33669778..33680825hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3811048
hg1911048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5758674
SamplesNA19076
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665969
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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