A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934236



Internal ID23556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75096000..75125000hg38UCSC Ensembl
chr3:75145151..75174151hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3829001
hg1929001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5447901
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934236
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004074


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