A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652189



Internal ID15388841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89425450..89459514hg38UCSC Ensembl
Innerchr9:92040365..92074429hg19UCSC Ensembl
Innerchr9:91230185..91264249hg18UCSC Ensembl
Innerchr9:89269919..89303983hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3834065
hg1934065
hg1834065
hg1734065
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517495
Supporting Variants
Samples
Known GenesSEMA4D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652189
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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