A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627853



Internal ID7014678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117404095..117412635hg38UCSC Ensembl
Innerchr11:117404095..117412635hg38UCSC Ensembl
Outerchr11:117403849..117412796hg38UCSC Ensembl
chr11:117274811..117283351hg19UCSC Ensembl
Innerchr11:117274811..117283351hg19UCSC Ensembl
Outerchr11:117274565..117283512hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg388541
hg198541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14292699
SamplesHG01198
Known GenesCEP164
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627853
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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