A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2619n223



Internal ID22805587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86925018..86926014hg38UCSC Ensembl
chr15:87468249..87469245hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6591707, nsv6581835
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2619n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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