A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193984



Internal ID20761024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86312076..86318301hg38UCSC Ensembl
chr15:86855307..86861532hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg386226
hg196226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500342
Supporting Variants
Samples
Known GenesAGBL1, AGBL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193984
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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