A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793017



Internal ID19170310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105737427..105790259hg38UCSC Ensembl
Innerchr13:106389776..106442608hg19UCSC Ensembl
Innerchr13:105187777..105240609hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3852833
hg1952833
hg1852833
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892442
Supporting Variants
Samples
Known GenesLINC00343
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793017
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