A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937895



Internal ID25978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107406264..107406497hg38UCSC Ensembl
chr3:107125111..107125344hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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