A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506966



Internal ID20880254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2639901..2686900hg38UCSC Ensembl
chr16:2689902..2736901hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3847000
hg1947000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179983
Samples
Known GenesERVK13-1, FLJ42627, KCTD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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