A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437332



Internal ID215923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73561566..73564524hg38UCSC Ensembl
chr3:73610717..73613675hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg382959
hg192959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936050
Samples
Known GenesPDZRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437332
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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