A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941263



Internal ID28216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167746903..167746903hg38UCSC Ensembl
chr3:167464691..167464691hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534672
Supporting Variants
Samples
Known GenesSERPINI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941263
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002344


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