A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563683



Internal ID336613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133969427..133971110hg38UCSC Ensembl
chr3:133688271..133689954hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937791
Samples
Known GenesSLCO2A1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563683
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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