A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935368



Internal ID24296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109328026..109328888hg38UCSC Ensembl
chr3:109046873..109047735hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437508
Supporting Variants
Samples
Known GenesDPPA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935368
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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