A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941601



Internal ID28421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159010955..159011119hg38UCSC Ensembl
chr3:158728744..158728908hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941601
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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