A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11069221



Internal ID4411598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90147616..90228716hg38UCSC Ensembl
chr3:90196766..90277866hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3881101
hg1981101
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596984
Supporting Variants
SamplesHG03926
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11069221
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