A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281121



Internal ID20848161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79675356..79676421hg38UCSC Ensembl
chr9:82290271..82291336hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575140
Supporting Variants
Samples
Known GenesTLE4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281121
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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