A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv182e214



Internal ID22756076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5193527..5224501hg38UCSC Ensembl
chr11:5214757..5245731hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3830975
hg1930975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3625212, esv3625213
SamplesHG03476, HG00581
Known GenesOR51V1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv182e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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