A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280099



Internal ID20847139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132438874..132439867hg38UCSC Ensembl
chr9:135314261..135315254hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571986
Supporting Variants
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280099
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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