A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501404



Internal ID20874637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24312276..24317766hg38UCSC Ensembl
chr16:24323597..24329087hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg385491
hg195491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180379
Samples
Known GenesCACNG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501404
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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