A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706018



Internal ID129684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56476685..56476834hg38UCSC Ensembl
chr16:56510597..56510746hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522837
Supporting Variants
Samples
Known GenesOGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706018
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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