A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281006



Internal ID20848047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76079292..76083062hg38UCSC Ensembl
chr9:78694208..78697978hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383771
hg193771
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567399
Supporting Variants
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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