A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452783



Internal ID230926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182008628..182013714hg38UCSC Ensembl
chr3:181726416..181731502hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg385087
hg195087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944709
Samples
Known GenesLOC100996490
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452783
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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