A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496422



Internal ID20869624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2482898..2485645hg38UCSC Ensembl
chr16:2532899..2535646hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382748
hg192748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029486
Samples
Known GenesTBC1D24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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