A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14160436



Internal ID3875065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55572982..55596815hg38UCSC Ensembl
chr11:55340458..55364291hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3823834
hg1923834
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626443
Supporting Variants
SamplesHG03517
Known GenesOR4C16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14160436
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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