A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944214



Internal ID30140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194938211..194941197hg38UCSC Ensembl
chr3:194658940..194661926hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382987
hg192987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944214
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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