A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16932321



Internal ID22270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43445996..43455687hg38UCSC Ensembl
chr3:43487488..43497179hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg389692
hg199692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450671
Supporting Variants
Samples
Known GenesANO10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16932321
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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