A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522130



Internal ID15449423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15660079..15689448hg38UCSC Ensembl
Innerchr17:15563393..15592762hg19UCSC Ensembl
Innerchr17:15504118..15533487hg18UCSC Ensembl
Innerchr17:15504118..15533487hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3829370
hg1929370
hg1829370
hg1729370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694903
Samples
Known GenesTRIM16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522130
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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