A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525332



Internal ID301496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93257318..93278470hg38UCSC Ensembl
chr15:93800547..93821699hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3821153
hg1921153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703740
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525332
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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