A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112289



Internal ID21295555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130960328..130979833hg38UCSC Ensembl
Innerchr9:133835715..133855220hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3819506
hg1919506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087939
Samplessample263
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112289
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