A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627856



Internal ID6668000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117525786..117530473hg38UCSC Ensembl
Innerchr11:117525786..117530473hg38UCSC Ensembl
Outerchr11:117525668..117530586hg38UCSC Ensembl
chr11:117396501..117401188hg19UCSC Ensembl
Innerchr11:117396501..117401188hg19UCSC Ensembl
Outerchr11:117396383..117401301hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384688
hg194688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14292704
SamplesHG03917
Known GenesDSCAML1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627856
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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