A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625626



Internal ID7012460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22927609..23086160hg38UCSC Ensembl
chr11:22949155..23107706hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38158552
hg19158552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14050710, essv14050711, essv14050709, essv14050712
SamplesNA19456, NA19445, NA19077, NA19338
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625626
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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