A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625623



Internal ID6665771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22803579..22866492hg38UCSC Ensembl
chr11:22825125..22888038hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3862914
hg1962914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14050687
SamplesNA19077
Known GenesCCDC179, GAS2, SVIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625623
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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