A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035984



Internal ID18778515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:4286176..4299636hg38UCSC Ensembl
Innerchr12:4395342..4408802hg19UCSC Ensembl
Innerchr12:4265603..4279063hg18UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3813461
hg1913461
hg1813461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1346n100
Supporting Variantsnssv3519808, nssv3518295
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)nsv1035984
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer