A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11068082



Internal ID3263121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89143782..89337641hg38UCSC Ensembl
chr3:89192932..89386791hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38193860
hg19193860
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596946
Supporting Variants
SamplesHG02882
Known GenesEPHA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11068082
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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