A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529326



Internal ID305351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67849397..67849714hg38UCSC Ensembl
chr16:67883300..67883617hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707533
Samples
Known GenesNUTF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529326
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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