A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451149



Internal ID229335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5404163..5407025hg38UCSC Ensembl
chr2:5544296..5547158hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg382863
hg192863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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