A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv882696



Internal ID16176652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:46366874..46396884hg38UCSC Ensembl
Innerchr18:43946837..43976847hg19UCSC Ensembl
Innerchr18:42200835..42230845hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3830011
hg1930011
hg1830011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576812
Supporting Variants
Samples
Known GenesRNF165
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv882696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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