A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442776



Internal ID221191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153881419..153896197hg38UCSC Ensembl
chr3:153599208..153613986hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3814779
hg1914779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442776
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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