A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589608



Internal ID18887889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35759275..35905870hg38UCSC Ensembl
Innerchr3:35800767..35947362hg19UCSC Ensembl
Innerchr3:35775771..35922366hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38146596
hg19146596
hg18146596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009026
Supporting Variants
Samples
Known GenesARPP21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589608
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