A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616087



Internal ID18567682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:343385..560798hg38UCSC Ensembl
Innerchr4:337174..554587hg19UCSC Ensembl
Innerchr4:327174..544587hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38217414
hg19217414
hg18217414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006781
Supporting Variants
Samples
Known GenesABCA11P, PIGG, ZNF141, ZNF721
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616087
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