A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980194



Internal ID54170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27456912..27457029hg38UCSC Ensembl
chr6:27424691..27424808hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458714
Supporting Variants
Samples
Known GenesZNF184
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980194
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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