A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116577



Internal ID21299843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85287656..85292443hg38UCSC Ensembl
Innerchr9:87902571..87907358hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg384788
hg194788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1242n145
Supporting Variantsnssv14089752
Samplessample160
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116577
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