A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3694818



Internal ID18993099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63555706..63722096hg38UCSC Ensembl
Innerchr9:68151440..68317830hg19UCSC Ensembl
Innerchr9:67641260..67807650hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38166391
hg19166391
hg18166391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035096
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3694818
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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