A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv212e214



Internal ID22756106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82153690..82171017hg38UCSC Ensembl
chr11:81864732..81882059hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3817328
hg1917328
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3626987, esv3626986
SamplesNA20762, HG01413, HG00281, HG00120, HG01757, HG02502, HG00154, HG02236, HG00101, HG01142, NA20538, HG03304, NA06994, NA20763, HG01509, HG01618
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv212e214
Frequency
Sample Size2504
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer