A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596961



Internal ID6637231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:89456470..89553389hg38UCSC Ensembl
chr3:89505620..89602539hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3896920
hg1996920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11068945
SamplesHG02882
Known GenesEPHA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596961
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