A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451375



Internal ID229558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127055978..127056050hg38UCSC Ensembl
chr3:126774821..126774893hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16939531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451375
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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