A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv217e214



Internal ID22756111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88005218..88090383hg38UCSC Ensembl
chr11:87738386..87823551hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3885166
hg1985166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3627139, esv3627141
SamplesHG01817, HG01807
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv217e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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