A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11068134



Internal ID3263279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89254791..89310265hg38UCSC Ensembl
chr3:89303941..89359415hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3855475
hg1955475
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596949
Supporting Variants
SamplesHG02882
Known GenesEPHA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11068134
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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