A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952666



Internal ID16954853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:46491689..46501188hg38UCSC Ensembl
Outerchr16:46525601..46535100hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000133
SamplesBILGI_BIOE
Known GenesANKRD26P1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952666
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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