A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633437



Internal ID7020246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105100858..105109710hg38UCSC Ensembl
Innerchr13:105100879..105109690hg38UCSC Ensembl
Outerchr13:105100838..105109731hg38UCSC Ensembl
chr13:105753209..105762061hg19UCSC Ensembl
Innerchr13:105753230..105762041hg19UCSC Ensembl
Outerchr13:105753189..105762082hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg388853
hg198853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14888784
SamplesNA18881
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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