A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027812



Internal ID20594852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86402817..86403581hg38UCSC Ensembl
chr15:86946048..86946812hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38765
hg19765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510899
Supporting Variants
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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