A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14241835



Internal ID4979374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94350682..94364837hg38UCSC Ensembl
chr11:94083848..94098003hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3814156
hg1914156
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627320
Supporting Variants
SamplesNA12890
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14241835
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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