A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3619473



Internal ID18571068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..66074hg38UCSC Ensembl
Innerchr4:12269..65966hg19UCSC Ensembl
Innerchr4:2269..55966hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3853806
hg1953698
hg1853698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005648
Supporting Variants
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3619473
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