A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984233



Internal ID56862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76472323..76472386hg38UCSC Ensembl
chr6:77182040..77182103hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984233
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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