A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438108



Internal ID15041339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:83873671..83927291hg38UCSC Ensembl
Innerchr9:86488586..86542206hg19UCSC Ensembl
Innerchr9:85678406..85732026hg18UCSC Ensembl
Innerchr9:81945705..81999325hg16UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3853621
hg1953621
hg1853621
hg1653621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470105
SamplesNA12872
Known GenesKIF27
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)nsv438108
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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