A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626568



Internal ID7013400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60805093..60806956hg38UCSC Ensembl
Innerchr11:60805093..60806956hg38UCSC Ensembl
Outerchr11:60804847..60807177hg38UCSC Ensembl
chr11:60572566..60574429hg19UCSC Ensembl
Innerchr11:60572566..60574429hg19UCSC Ensembl
Outerchr11:60572320..60574650hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381864
hg191864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14176253, essv14176254
SamplesHG01187, HG01414
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626568
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