A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515615



Internal ID292096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31505060..31506470hg38UCSC Ensembl
chr16:31516381..31517791hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707302
Samples
Known GenesC16orf58
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515615
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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