A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059292



Internal ID19148511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44215944..44394853hg38UCSC Ensembl
Innerchr18:41795909..41974818hg19UCSC Ensembl
Innerchr18:40049907..40228816hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38178910
hg19178910
hg18178910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726067
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)nsv1059292
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