A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582968



Internal ID18534563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:151258123..151536426hg38UCSC Ensembl
Innerchr2:152114637..152392940hg19UCSC Ensembl
Innerchr2:151822883..152101186hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38278304
hg19278304
hg18278304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011339
Supporting Variants
Samples
Known GenesMIR4773-1, MIR4773-2, NEB, NMI, RBM43, RIF1, TNFAIP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582968
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