A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591336



Internal ID20964407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85644389..85644698hg38UCSC Ensembl
chr15:86187620..86187929hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240490
Samples
Known GenesAKAP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591336
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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