A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517219



Internal ID293645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86987447..86987788hg38UCSC Ensembl
chr15:87530678..87531019hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705449
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517219
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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