A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892042



Internal ID168885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:163950241..164098181hg38UCSC Ensembl
chr1:163919478..164067418hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38147941
hg19147941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892042
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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