A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661826



Internal ID9581245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119649385..119652407hg38UCSC Ensembl
Outerchr11:119649228..119652560hg38UCSC Ensembl
Innerchr11:119520095..119523117hg19UCSC Ensembl
Outerchr11:119519938..119523270hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6141183, essv6112882, essv5887613, essv6144391
SamplesNA12249, HG01174, NA20803, NA19346
Known GenesPVRL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661826
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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