A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013303



Internal ID19102521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:193051589..193321946hg38UCSC Ensembl
Innerchr2:193916315..194186671hg19UCSC Ensembl
Innerchr2:193624560..193894916hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38270358
hg19270357
hg18270357
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729311
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013303
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