A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969797



Internal ID47181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134129827..134149511hg38UCSC Ensembl
chr6:134450965..134470649hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3819685
hg1919685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969797
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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