A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279635



Internal ID20846675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113112798..113131795hg38UCSC Ensembl
chr9:115875078..115894075hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3818998
hg1918998
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565161
Supporting Variants
Samples
Known GenesFAM225A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279635
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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