A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695050



Internal ID18646645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111664365..111716743hg38UCSC Ensembl
Innerchr9:114426645..114479023hg19UCSC Ensembl
Innerchr9:113466466..113518844hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3852379
hg1952379
hg1852379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053111
Supporting Variants
Samples
Known GenesC9orf84, DNAJC25-GNG10, GNG10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695050
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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