A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626711



Internal ID7013541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67444873..67448725hg38UCSC Ensembl
Innerchr11:67444877..67448721hg38UCSC Ensembl
Outerchr11:67444869..67448729hg38UCSC Ensembl
chr11:67212344..67216196hg19UCSC Ensembl
Innerchr11:67212348..67216192hg19UCSC Ensembl
Outerchr11:67212340..67216200hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383853
hg193853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14197544, essv14197545
SamplesNA19332, NA19036
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626711
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