A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517634



Internal ID294050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62794470..62807392hg38UCSC Ensembl
chr16:62828374..62841296hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3812923
hg1912923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517634
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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