A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626503



Internal ID7013335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57245111..57250743hg38UCSC Ensembl
Innerchr11:57245143..57250712hg38UCSC Ensembl
Outerchr11:57245080..57250775hg38UCSC Ensembl
chr11:57012585..57018217hg19UCSC Ensembl
Innerchr11:57012617..57018186hg19UCSC Ensembl
Outerchr11:57012554..57018249hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg385633
hg195633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14168696
SamplesHG03369
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626503
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