A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229062



Internal ID20796102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9630441..9631632hg38UCSC Ensembl
chr11:9651988..9653179hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00024


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