A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235845



Internal ID20802885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32467553..32467749hg38UCSC Ensembl
chr13:33041690..33041886hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592082
Supporting Variants
Samples
Known GenesN4BP2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235845
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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