A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510640



Internal ID20883961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54209949..54218150hg38UCSC Ensembl
chr16:54243861..54252062hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg388202
hg198202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510640
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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