A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954466



Internal ID36968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105709626..105709696hg38UCSC Ensembl
chr4:106630783..106630853hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468510
Supporting Variants
Samples
Known GenesGSTCD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954466
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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