A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945963



Internal ID31315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195368939..195370784hg38UCSC Ensembl
chr3:195089668..195091513hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381846
hg191846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449779
Supporting Variants
Samples
Known GenesACAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945963
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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