A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452620



Internal ID230767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:221897043..221922703hg38UCSC Ensembl
chr2:222761763..222787422hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3825661
hg1925660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16928346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452620
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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