A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934191



Internal ID23531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71685724..71685756hg38UCSC Ensembl
chr3:71734875..71734907hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534192
Supporting Variants
Samples
Known GenesEIF4E3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934191
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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