A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518886



Internal ID15446179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:165744950..165772409hg38UCSC Ensembl
Innerchr1:165714187..165741646hg19UCSC Ensembl
Innerchr1:163980811..164008270hg18UCSC Ensembl
Innerchr1:162445845..162473304hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3827460
hg1927460
hg1827460
hg1727460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696345
Samples
Known GenesTMCO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518886
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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