A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594600



Internal ID20967671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86128248..86627037hg38UCSC Ensembl
chr15:86671479..87170268hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38498790
hg19498790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240501
Samples
Known GenesAGBL1, AGBL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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