A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944275



Internal ID30185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196563589..196563592hg38UCSC Ensembl
chr3:196290460..196290463hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547170
Supporting Variants
Samples
Known GenesWDR53
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944275
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.011654


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