A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525192



Internal ID301365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79730777..79746467hg38UCSC Ensembl
chr15:80023119..80038809hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3815691
hg1915691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525192
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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