A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709484



Internal ID133150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57569072..57569478hg38UCSC Ensembl
chr16:57602984..57603390hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515109
Supporting Variants
Samples
Known GenesGPR114
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709484
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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