A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935053



Internal ID24097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70433544..70441019hg38UCSC Ensembl
chr3:70482695..70490170hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg387476
hg197476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935053
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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