A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219900



Internal ID20786940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29944407..29944899hg38UCSC Ensembl
chr13:30518544..30519036hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590095
Supporting Variants
Samples
Known GenesLINC00544
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219900
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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