A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518978



Internal ID15446271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87840771..87854928hg38UCSC Ensembl
Innerchr9:90455686..90469843hg19UCSC Ensembl
Innerchr9:89645506..89659663hg18UCSC Ensembl
Innerchr9:87685240..87699397hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3814158
hg1914158
hg1814158
hg1714158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694294
Samples
Known GenesCTSLP8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518978
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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