A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv214e214



Internal ID22756108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83845752..83890278hg38UCSC Ensembl
chr11:83556795..83601321hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3844527
hg1944527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3627028, esv3627027
SamplesNA18536, HG00580, HG01846, HG00581
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv214e214
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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