A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632614



Internal ID7019424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69188337..69236248hg38UCSC Ensembl
chr13:69762469..69810380hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3847912
hg1947912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14786064
SamplesNA19916
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632614
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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