A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110762



Internal ID21294028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:117366006..117368505hg38UCSC Ensembl
Innerchr1:117908628..117911127hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14097087, nssv14097558
Samplessample349, sample348
Known GenesMAN1A2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110762
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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