A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661413



Internal ID15398065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:31890473..31893895hg38UCSC Ensembl
Innerchr20:30478276..30481698hg19UCSC Ensembl
Innerchr20:29941937..29945359hg18UCSC Ensembl
Innerchr20:29941937..29945359hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383423
hg193423
hg183423
hg173423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517635
Supporting Variants
Samples
Known GenesTTLL9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661413
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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