A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112013



Internal ID21295279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:106485633..106487504hg38UCSC Ensembl
Innerchr1:107028255..107030126hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg381872
hg191872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104330
Samplessample75
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112013
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