A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5445796



Internal ID224138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13227645..13229470hg38UCSC Ensembl
chr3:13269145..13270970hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16929502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5445796
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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