A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436754



Internal ID215362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20937780..20953901hg38UCSC Ensembl
chr3:20979272..20995393hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3816122
hg1916122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436754
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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