A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv166e214



Internal ID22756060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111409067..111472578hg38UCSC Ensembl
chr10:113168825..113232336hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3863512
hg1963512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3624558, esv3624561
SamplesNA19379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv166e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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