A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442633



Internal ID221055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184697863..184710137hg38UCSC Ensembl
chr3:184415651..184427925hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3812275
hg1912275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16943045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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