A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627826



Internal ID7014651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116562095..116569625hg38UCSC Ensembl
Innerchr11:116562595..116569125hg38UCSC Ensembl
Outerchr11:116561095..116570625hg38UCSC Ensembl
chr11:116432812..116440342hg19UCSC Ensembl
Innerchr11:116433312..116439842hg19UCSC Ensembl
Outerchr11:116431812..116441342hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg387531
hg197531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14291034
SamplesHG03484
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627826
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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