A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437675



Internal ID216260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135644383..135648219hg38UCSC Ensembl
chr3:135363225..135367061hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg383837
hg193837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437675
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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