A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505060



Internal ID18456655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:4286176..4299507hg38UCSC Ensembl
Innerchr12:4395342..4408673hg19UCSC Ensembl
Innerchr12:4265603..4278934hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3813332
hg1913332
hg1813332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037515
Supporting Variants
Samples
Known GenesCCND2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505060
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