A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929519



Internal ID20409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13514617..13514701hg38UCSC Ensembl
chr3:13556117..13556201hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929519
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004685


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