A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945950



Internal ID31308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195187075..195187100hg38UCSC Ensembl
chr3:194907804..194907829hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540246
Supporting Variants
Samples
Known GenesXXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945950
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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