A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv201e214



Internal ID20121624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60084926..60104676hg38UCSC Ensembl
chr11:59852399..59872149hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3819751
hg1919751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3626548, esv3626547
SamplesNA18952, HG03786, NA18864, NA18946
Known GenesMS4A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv201e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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