A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936898



Internal ID25315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103305374..103305432hg38UCSC Ensembl
chr3:103024218..103024276hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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