A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520152



Internal ID296489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3674968..3675141hg38UCSC Ensembl
chr16:3724969..3725142hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706386
Samples
Known GenesTRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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