A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525386



Internal ID301548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46920733..46920909hg38UCSC Ensembl
chr16:46954645..46954821hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17709345
Samples
Known GenesGPT2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525386
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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