A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597867



Internal ID6638134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135139775..135371927hg38UCSC Ensembl
chr3:134858617..135090769hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38232153
hg19232153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11156527
SamplesNA18520
Known GenesEPHB1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597867
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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