A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14204900



Internal ID6215852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69129050..69133927hg38UCSC Ensembl
Innerchr11:69129071..69133907hg38UCSC Ensembl
Outerchr11:69129030..69133948hg38UCSC Ensembl
chr11:68896518..68901395hg19UCSC Ensembl
Innerchr11:68896539..68901375hg19UCSC Ensembl
Outerchr11:68896498..68901416hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg384878
hg194878
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626743
Supporting Variants
SamplesNA19741
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14204900
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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