A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10977915



Internal ID3905879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32797206..32807757hg38UCSC Ensembl
chr3:32838698..32849249hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3810552
hg1910552
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595783
Supporting Variants
SamplesHG03559
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10977915
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