A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694942



Internal ID15084908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16020395..16244507hg38UCSC Ensembl
Innerchr17:15923709..16147821hg19UCSC Ensembl
Innerchr17:15864434..16088546hg18UCSC Ensembl
Innerchr17:15864434..16088546hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38224113
hg19224113
hg18224113
hg17224113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522169
Supporting Variants
Samples
Known GenesNCOR1, PIGL, TTC19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694942
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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