A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14786064



Internal ID6315694
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3632614
Supporting Variants
SamplesNA19916
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14786064
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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