A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632966



Internal ID7019776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85130639..85274498hg38UCSC Ensembl
chr13:85704774..85848633hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38143860
hg19143860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822761
SamplesHG03755
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632966
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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