A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446909



Internal ID225227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:225664873..225665663hg38UCSC Ensembl
chr2:226529589..226530379hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16928405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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