A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525972



Internal ID302119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67815632..67817269hg38UCSC Ensembl
chr16:67849535..67851172hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381638
hg191638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707530
Samples
Known GenesTSNAXIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525972
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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