A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787800



Internal ID19166638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:64709515..65010859hg38UCSC Ensembl
Innerchr13:65283647..65584991hg19UCSC Ensembl
Innerchr13:64181648..64482992hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38301345
hg19301345
hg18301345
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892373
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=66
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787800
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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