A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437186



Internal ID215782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23047357..23050609hg38UCSC Ensembl
chr3:23088848..23092100hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383253
hg193253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437186
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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