A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626764



Internal ID7013594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70253747..70256614hg38UCSC Ensembl
Innerchr11:70253797..70256564hg38UCSC Ensembl
Outerchr11:70253684..70256677hg38UCSC Ensembl
chr11:70099853..70102720hg19UCSC Ensembl
Innerchr11:70099903..70102670hg19UCSC Ensembl
Outerchr11:70099790..70102783hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg382868
hg192868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14207809, essv14207810
SamplesNA19072, HG02654
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626764
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