A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501419



Internal ID20874652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10611659..10625332hg38UCSC Ensembl
chr16:10705516..10719189hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3813674
hg1913674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501419
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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