A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560640



Internal ID333643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140294558..140747260hg38UCSC Ensembl
chr3:140013400..140466102hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38452703
hg19452703
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939697
Samples
Known GenesCLSTN2, CLSTN2-AS1, TRIM42
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560640
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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