A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632876



Internal ID7019687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81798208..81873865hg38UCSC Ensembl
chr13:82372343..82448000hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3875658
hg1975658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14820062, essv14820061
SamplesHG02819, HG01883
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632876
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer