A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528985



Internal ID305022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20703170..20714693hg38UCSC Ensembl
chr16:20714492..20726015hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3811524
hg1911524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528985
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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