A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833295



Internal ID6159019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:79568878..79726768hg19UCSC Ensembl
Outerchr16:78126379..78284269hg18UCSC Ensembl
Outerchr16:78126379..78284269hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1452882
Samples
Known GenesMAF
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833295
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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