A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220999



Internal ID20788039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110902026..110902236hg38UCSC Ensembl
chr13:111554373..111554583hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583052
Supporting Variants
Samples
Known GenesANKRD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220999
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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