A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560290



Internal ID333301
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 StatusM
Merged Variants
Supporting Variantsnssv16978013
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560290
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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