A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946215



Internal ID22721702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86985775..86986587hg38UCSC Ensembl
chr15:87529006..87529818hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383243
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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