A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3551106



Internal ID18752182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111697176..111697351hg38UCSC Ensembl
chr13:112349523..112349698hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9749853
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3551106
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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