A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518620



Internal ID15445913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15660079..15704880hg38UCSC Ensembl
Innerchr17:15563393..15608194hg19UCSC Ensembl
Innerchr17:15504118..15548919hg18UCSC Ensembl
Innerchr17:15504118..15548919hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3844802
hg1944802
hg1844802
hg1744802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696068
Samples
Known GenesTRIM16, ZNF286A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518620
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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