A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011954



Internal ID22073585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:49471356..49476982hg38UCSC Ensembl
Outerchr18:49468535..49483097hg38UCSC Ensembl
Innerchr18:46997726..47003352hg19UCSC Ensembl
Outerchr18:46994905..47009467hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3814563
hg1914563
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155514
Supporting Variants
Samples
Known GenesC18orf32, RPL17-C18orf32
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011954
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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