A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892417



Internal ID169140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161576587..161662587hg38UCSC Ensembl
chr1:161546377..161632377hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3886001
hg1986001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421696
Supporting Variants
Samples
Known GenesFCGR2C, FCGR3B, HSPA7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892417
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.072013


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