A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532398



Internal ID308322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52791572..52795177hg38UCSC Ensembl
chr15:53083769..53087374hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383606
hg193606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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