A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500680



Internal ID20873908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:470269..551898hg38UCSC Ensembl
chr16:520269..601898hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3881630
hg1981630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192996
Samples
Known GenesCAPN15, LINC00235, MIR3176, MIR5587, RAB11FIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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