A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517725



Internal ID294139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58226903..58292667hg38UCSC Ensembl
chr15:58519102..58584866hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865765
hg1965765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517725
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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