A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449389



Internal ID227625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19628015..19636584hg38UCSC Ensembl
chr2:19827776..19836345hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg388570
hg198570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449389
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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