A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113569



Internal ID21296835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80854255..80936071hg38UCSC Ensembl
Innerchr1:81319940..81401756hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3881817
hg1981817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089848
Samplessample268
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113569
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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