A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514165



Internal ID20887517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55713739..55723137hg38UCSC Ensembl
chr16:55747651..55757049hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg389399
hg199399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514165
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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