A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531053



Internal ID307016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67127980..67128095hg38UCSC Ensembl
chr16:67161883..67161998hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707481
Samples
Known GenesC16orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531053
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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