A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438277



Internal ID15388087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26786524..26788009hg38UCSC Ensembl
Innerchr18:24366488..24367973hg19UCSC Ensembl
Innerchr18:22620486..22621971hg18UCSC Ensembl
Innerchr18:22618475..22619960hg16UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381486
hg191486
hg181486
hg161486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470690
SamplesNA19171
Known Genes
MethodSNP array
AnalysisNull genotypes - for each genotype assay and population sample we defined the null genotype pattern of that assay as the binary vector (length 90) of null genotype calls across the 90 individuals.
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nsv438277
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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