A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449957



Internal ID228177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32903555..32940509hg38UCSC Ensembl
chr3:32945047..32982001hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3836955
hg1936955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv345n206
Supporting Variantsnssv16932398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449957
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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