A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220684



Internal ID20787724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105633365..105833042hg38UCSC Ensembl
chr13:106285714..106485391hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38199678
hg19199678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581764
Supporting Variants
Samples
Known GenesLINC00343
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220684
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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