A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449365



Internal ID227604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4073830..4120314hg38UCSC Ensembl
chr3:4115514..4161998hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3846485
hg1946485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929284
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449365
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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