A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440826



Internal ID219324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116167995..116183230hg38UCSC Ensembl
chr3:115886842..115902077hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3815236
hg1915236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938437
Samples
Known GenesLSAMP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440826
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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