A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244096



Internal ID20811136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13777095..13779081hg38UCSC Ensembl
chr18:13777094..13779080hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381987
hg191987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585409
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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