A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626991



Internal ID7013821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82212456..82340919hg38UCSC Ensembl
chr11:81923498..82051961hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38128464
hg19128464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv213e214
Supporting Variantsessv14218754, essv14218753
SamplesNA20771, NA18988
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626991
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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