A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939390



Internal ID26971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140767219..140779066hg38UCSC Ensembl
chr3:140486061..140497908hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3811848
hg1911848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447618
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939390
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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