A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117064



Internal ID21300330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:185322574..185351944hg38UCSC Ensembl
Innerchr1:185291706..185321076hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3829371
hg1929371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089527
Samplessample239
Known GenesLOC100288079
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117064
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