A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16942261



Internal ID28855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160426572..160426679hg38UCSC Ensembl
chr3:160144360..160144467hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434048
Supporting Variants
Samples
Known GenesSMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16942261
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002498


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