A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533708



Internal ID309592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73713030..73713091hg38UCSC Ensembl
chr15:74005371..74005432hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701036
Samples
Known GenesCD276
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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