A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111427



Internal ID21294693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2881902..2890737hg38UCSC Ensembl
Innerchr9:2881902..2890737hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg388836
hg198836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087956, nssv14090841
Samplessample203, sample270
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111427
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