A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626191



Internal ID6666340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46651662..46681651hg38UCSC Ensembl
chr11:46673212..46703201hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3829990
hg1929990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14118999
SamplesNA20866
Known GenesARHGAP1, ATG13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626191
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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