A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14207810



Internal ID5659839
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626764
Supporting Variants
SamplesNA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14207810
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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