A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706776



Internal ID130442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2472436..2472513hg38UCSC Ensembl
chr16:2522437..2522514hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520791
Supporting Variants
Samples
Known GenesNTN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706776
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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