A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625182



Internal ID7012017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4368636..4429909hg38UCSC Ensembl
chr11:4389866..4451139hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861274
hg1961274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv181e214
Supporting Variantsessv13998741, essv13998742
SamplesHG03126, HG03132
Known GenesTRIM21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625182
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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