A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14204907



Internal ID6051523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69281604..69288877hg38UCSC Ensembl
Innerchr11:69281604..69288877hg38UCSC Ensembl
Outerchr11:69281399..69289072hg38UCSC Ensembl
chr11:69049071..69056344hg19UCSC Ensembl
Innerchr11:69049071..69056344hg19UCSC Ensembl
Outerchr11:69048866..69056539hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg387274
hg197274
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626746
Supporting Variants
SamplesNA19448
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14204907
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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