A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564171



Internal ID18515766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:32687193..32724472hg38UCSC Ensembl
Innerchr18:30267156..30304435hg19UCSC Ensembl
Innerchr18:28521154..28558433hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3837280
hg1937280
hg1837280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060732
Supporting Variants
Samples
Known GenesKLHL14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564171
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