A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452669



Internal ID230815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9707676..9709149hg38UCSC Ensembl
chr3:9749360..9750833hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381474
hg191474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930850
Samples
Known GenesCPNE9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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