A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16934779



Internal ID23922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67385378..67393735hg38UCSC Ensembl
chr3:67435802..67444159hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg388358
hg198358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451587
Supporting Variants
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16934779
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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