A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709482



Internal ID133148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57568438..57569480hg38UCSC Ensembl
chr16:57602350..57603392hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381043
hg191043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517648
Supporting Variants
Samples
Known GenesGPR114
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709482
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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