A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625939



Internal ID6666087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35793044..35804167hg38UCSC Ensembl
chr11:35814594..35825717hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3811124
hg1911124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14090433
SamplesNA20886
Known GenesTRIM44
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625939
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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