A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239667



Internal ID20806707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71924257..71924819hg38UCSC Ensembl
chr15:72216598..72217160hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593577
Supporting Variants
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00016


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