A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518068



Internal ID15445361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60028812..60040758hg38UCSC Ensembl
Innerchr18:57696044..57707990hg19UCSC Ensembl
Innerchr18:55847024..55858970hg18UCSC Ensembl
Innerchr18:55847024..55858970hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3811947
hg1911947
hg1811947
hg1711947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695481
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518068
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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