A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930810



Internal ID21290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9489770..9490239hg38UCSC Ensembl
chr3:9531454..9531923hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930810
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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