A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937244



Internal ID25541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105886449..105886449hg38UCSC Ensembl
chr3:105605296..105605296hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937244
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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