A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525976



Internal ID15453269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47549961..48001115hg38UCSC Ensembl
Innerchr16:47583872..48035026hg19UCSC Ensembl
Innerchr16:46141373..46592527hg18UCSC Ensembl
Innerchr16:46141373..46592527hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38451155
hg19451155
hg18451155
hg17451155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702195
Samples
Known GenesPHKB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525976
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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