A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv192e214



Internal ID22756086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37742851..37823206hg38UCSC Ensembl
chr11:37764401..37844756hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3880356
hg1980356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3625990, esv3625989
SamplesHG01402, NA20863, NA20796, NA19657, HG02221, HG02314, NA19786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv192e214
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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