A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239435



Internal ID20806475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28320029..28591568hg38UCSC Ensembl
chr15:28565175..28836714hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38271540
hg19271540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589377
Supporting Variants
Samples
Known GenesGOLGA8F, GOLGA8G, HERC2, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239435
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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