A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524813



Internal ID18823094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:90056944..90098285hg38UCSC Ensembl
Innerchr12:90450721..90492062hg19UCSC Ensembl
Innerchr12:88974852..89016193hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg3841342
hg1941342
hg1841342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053151
Supporting Variants
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)nssv3524813
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