A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989525



Internal ID60439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158803983..158804135hg38UCSC Ensembl
chr6:159225015..159225167hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472852
Supporting Variants
Samples
Known GenesEZR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989525
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002966


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