A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115893



Internal ID21299159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:118890924..118894146hg38UCSC Ensembl
Innerchr6:119212088..119215310hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383223
hg193223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083070
Samplessample353
Known GenesASF1A, MCM9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115893
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