A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv219e214



Internal ID20121642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90227976..90288834hg38UCSC Ensembl
chr11:89961144..90022002hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3860859
hg1960859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3627194, esv3627196, esv3627193
SamplesHG02561, HG00146
Known GenesDISC1FP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv219e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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