A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632559



Internal ID7019369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67540483..67579048hg38UCSC Ensembl
chr13:68114615..68153180hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3838566
hg1938566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14781084, essv14781085
SamplesHG04158, HG02756
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632559
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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