A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16982377



Internal ID55599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26368000..26406000hg38UCSC Ensembl
chr6:26368228..26406228hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3838001
hg1938001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466978
Supporting Variants
Samples
Known GenesBTN2A2, BTN3A1, BTN3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16982377
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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