A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632967



Internal ID7019777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85136312..85219025hg38UCSC Ensembl
chr13:85710447..85793160hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3882714
hg1982714
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14822762
SamplesHG03755
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632967
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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