A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5652333



Internal ID9024732
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 StatusS
Merged Variantsesv2661821
Supporting Variants
SamplesHG00650
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5652333
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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