A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941860



Internal ID28598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170947169..170961114hg38UCSC Ensembl
chr3:170664958..170678903hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3813946
hg1913946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437287
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941860
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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