A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941017



Internal ID28049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:144045058..144046943hg38UCSC Ensembl
chr3:143763900..143765785hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381886
hg191886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941017
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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