A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990639



Internal ID61174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167651333..167652028hg38UCSC Ensembl
chr6:168052013..168052708hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5469465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.93147


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