A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514204



Internal ID290704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15842207..15842350hg38UCSC Ensembl
chr21:17214526..17214669hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17734117
Samples
Known GenesUSP25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514204
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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