A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931696



Internal ID21867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44474400..44475238hg38UCSC Ensembl
chr3:44515892..44516730hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38839
hg19839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443641
Supporting Variants
Samples
Known GenesZNF445
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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