A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16940336



Internal ID27603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141058122..141059835hg38UCSC Ensembl
chr3:140776964..140778677hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381714
hg191714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436330
Supporting Variants
Samples
Known GenesSPSB4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16940336
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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