A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5447408



Internal ID225712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106019425..106019540hg38UCSC Ensembl
chr3:105738272..105738387hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5447408
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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