A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596266



Internal ID18547861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84947861..84985130hg38UCSC Ensembl
Innerchr3:84997012..85034281hg19UCSC Ensembl
Innerchr3:85079702..85116971hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3837270
hg1937270
hg1837270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010140
Supporting Variants
Samples
Known GenesCADM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596266
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