A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14268099



Internal ID3136184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105072107..105104164hg38UCSC Ensembl
chr11:104942834..104974891hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3832058
hg1932058
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627605
Supporting Variants
SamplesHG02763
Known GenesCARD17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14268099
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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