A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661821



Internal ID9927926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134091576..134093119hg38UCSC Ensembl
Outerchr3:134091539..134093169hg38UCSC Ensembl
Innerchr3:133810420..133811963hg19UCSC Ensembl
Outerchr3:133810383..133812013hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg381631
hg191631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5652333
SamplesHG00650
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661821
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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