A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628050



Internal ID6668194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128857623..128868844hg38UCSC Ensembl
Innerchr11:128857623..128868844hg38UCSC Ensembl
Outerchr11:128857576..128868954hg38UCSC Ensembl
chr11:128727518..128738739hg19UCSC Ensembl
Innerchr11:128727518..128738739hg19UCSC Ensembl
Outerchr11:128727471..128738849hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811222
hg1911222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14308936
SamplesHG01277
Known GenesKCNJ1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628050
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