A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517428



Internal ID15444721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135257320..135469324hg38UCSC Ensembl
Innerchr9:138149166..138361170hg19UCSC Ensembl
Innerchr9:137288987..137500991hg18UCSC Ensembl
Innerchr9:135375111..135587115hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38212005
hg19212005
hg18212005
hg17212005
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703715, nssv696539, nssv705895, nssv658114, nssv652001, nssv655985, nssv681068
Samples
Known GenesC9orf62, PPP1R26-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517428
Frequency
Sample Size2026
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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