A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978013



Internal ID52746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3280492..3281158hg38UCSC Ensembl
chr6:3280726..3281392hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560290
Supporting Variants
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978013
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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