A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5439069



Internal ID217615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189285936..189287558hg38UCSC Ensembl
chr3:189003725..189005347hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381623
hg191623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16944914
Samples
Known GenesTPRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5439069
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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