A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497446



Internal ID20870652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34189801..34214000hg38UCSC Ensembl
chr16:33992268..34016467hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3824200
hg1924200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2808n223
Supporting Variantsnssv18194288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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