A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886400



Internal ID16180356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67942742..68116409hg38UCSC Ensembl
Innerchr18:65609979..65783646hg19UCSC Ensembl
Innerchr18:63760959..63934626hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38173668
hg19173668
hg18173668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577327
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv886400
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