A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11068759



Internal ID6019656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89318575..89412084hg38UCSC Ensembl
chr3:89367725..89461234hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3893510
hg1993510
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596951
Supporting Variants
SamplesNA19431
Known GenesEPHA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11068759
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer