A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11068975



Internal ID3263177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89490665..89747933hg38UCSC Ensembl
chr3:89539815..89797083hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38257269
hg19257269
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596964
Supporting Variants
SamplesHG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11068975
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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