A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114232



Internal ID21297498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26109733..26112817hg38UCSC Ensembl
Innerchr1:26436224..26439308hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383085
hg193085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098193
Samplessample357
Known GenesPDIK1L
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114232
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