A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603516



Internal ID6990547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185998891..186097893hg38UCSC Ensembl
chr4:186920045..187019047hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3899003
hg1999003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11741707, essv11741706, essv11741703, essv11741704, essv11741701, essv11741708, essv11741709, essv11741702, essv11741705
SamplesHG03731, HG02727, HG04156, HG04183, HG03771, HG04180, HG03951, NA20847, HG03864
Known GenesTLR3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603516
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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