A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449153



Internal ID227398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99273287..99289574hg38UCSC Ensembl
chr3:98992131..99008418hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3816288
hg1916288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449153
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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