A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625864



Internal ID7012698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32562120..32581321hg38UCSC Ensembl
chr11:32583666..32602867hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3819202
hg1919202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14084228
SamplesHG01550
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625864
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