A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449367



Internal ID227606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132172331..132172392hg38UCSC Ensembl
chr3:131891175..131891236hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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