A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436882



Internal ID215490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26181566..26390730hg38UCSC Ensembl
chr3:26223057..26432221hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38209165
hg19209165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436882
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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