A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628052



Internal ID7014877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128950978..128951778hg38UCSC Ensembl
Innerchr11:128950996..128951761hg38UCSC Ensembl
Outerchr11:128950961..128951796hg38UCSC Ensembl
chr11:128820873..128821673hg19UCSC Ensembl
Innerchr11:128820891..128821656hg19UCSC Ensembl
Outerchr11:128820856..128821691hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14308939
SamplesHG00284
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628052
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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