A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626883



Internal ID7013713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77519155..77521823hg38UCSC Ensembl
Innerchr11:77519163..77521815hg38UCSC Ensembl
Outerchr11:77519147..77521831hg38UCSC Ensembl
chr11:77230200..77232868hg19UCSC Ensembl
Innerchr11:77230208..77232860hg19UCSC Ensembl
Outerchr11:77230192..77232876hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382669
hg192669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214809, essv14214808
SamplesNA20811, NA20786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626883
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer