A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892680



Internal ID18836814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42965277..43092949hg38UCSC Ensembl
Outerchr15:42965277..43092949hg38UCSC Ensembl
Innerchr15:43257475..43385147hg19UCSC Ensembl
Outerchr15:43257475..43385147hg19UCSC Ensembl
Innerchr15:41044767..41172439hg18UCSC Ensembl
Outerchr15:41044767..41172439hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38127673
hg19127673
hg18127673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784819
Samples
Known GenesUBR1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892680
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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