A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632898



Internal ID7019709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82899119..82916584hg38UCSC Ensembl
chr13:83473254..83490719hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3817466
hg1917466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14821619
SamplesHG04060
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632898
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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