A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941409



Internal ID28306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173140832..173140904hg38UCSC Ensembl
chr3:172858622..172858694hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445205
Supporting Variants
Samples
Known GenesSPATA16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941409
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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