A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500332



Internal ID20873558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86333858..86343539hg38UCSC Ensembl
chr15:86877089..86886770hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg389682
hg199682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027806
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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