A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664627



Internal ID9930732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32916512..32922635hg38UCSC Ensembl
Outerchr3:32916475..32922685hg38UCSC Ensembl
Innerchr3:32958004..32964127hg19UCSC Ensembl
Outerchr3:32957967..32964177hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg386211
hg196211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5865801
SamplesHG00281
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664627
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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