A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626612



Internal ID7013444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62679843..62680601hg38UCSC Ensembl
Innerchr11:62679893..62680551hg38UCSC Ensembl
Outerchr11:62679763..62680681hg38UCSC Ensembl
chr11:62447315..62448073hg19UCSC Ensembl
Innerchr11:62447365..62448023hg19UCSC Ensembl
Outerchr11:62447235..62448153hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14179726
SamplesHG03105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626612
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