A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626695



Internal ID7013526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66536641..66537696hg38UCSC Ensembl
Innerchr11:66536641..66537696hg38UCSC Ensembl
Outerchr11:66536310..66538035hg38UCSC Ensembl
chr11:66304112..66305167hg19UCSC Ensembl
Innerchr11:66304112..66305167hg19UCSC Ensembl
Outerchr11:66303781..66305506hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14195759, essv14195762, essv14195769, essv14195771, essv14195765, essv14195766, essv14195768, essv14195773, essv14195764, essv14195761, essv14195767, essv14195770, essv14195760, essv14195763, essv14195772
SamplesHG00189, HG02312, HG01110, NA20910, NA12761, NA20862, HG00275, HG00276, HG00146, NA20522, HG01685, HG01912, HG00288, HG01914, NA19676
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626695
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer