A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170190



Internal ID21314251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:46175878..46244149hg38UCSC Ensembl
Outerchr18:46168395..46251091hg38UCSC Ensembl
Innerchr18:43755844..43824115hg19UCSC Ensembl
Outerchr18:43748361..43831057hg19UCSC Ensembl
Innerchr18:42009842..42078113hg18UCSC Ensembl
Outerchr18:42002359..42085055hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3882697
hg1982697
hg1882697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249441
SamplesPML_1
Known GenesC18orf25
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170190
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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