A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526404



Internal ID15453697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29186142..29188221hg38UCSC Ensembl
Innerchr18:26766107..26768186hg19UCSC Ensembl
Innerchr18:25020105..25022184hg18UCSC Ensembl
Innerchr18:25020105..25022184hg17UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg382080
hg192080
hg182080
hg172080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702704
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526404
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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