A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14280570



Internal ID6906705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109707443..109746858hg38UCSC Ensembl
chr11:109578169..109617584hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3839416
hg1939416
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627709
Supporting Variants
SamplesNA21112
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14280570
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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