A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231780



Internal ID20798820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106855026..106855465hg38UCSC Ensembl
chr13:107507374..107507813hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231780
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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