A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586876



Internal ID7058258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17988456..17989741hg38UCSC Ensembl
Innerchr19:18099265..18100550hg19UCSC Ensembl
Innerchr19:17960265..17961550hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381286
hg191286
hg181286
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991938
Supporting Variants
SamplesHuRef
Known GenesKCNN1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586876
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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