A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627965



Internal ID7014790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123759836..123761861hg38UCSC Ensembl
Innerchr11:123759886..123761811hg38UCSC Ensembl
Outerchr11:123759786..123761911hg38UCSC Ensembl
chr11:123630544..123632569hg19UCSC Ensembl
Innerchr11:123630594..123632519hg19UCSC Ensembl
Outerchr11:123630494..123632619hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382026
hg192026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14301550
SamplesHG00599
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627965
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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