A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223725



Internal ID20790765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49190935..49192077hg38UCSC Ensembl
chr11:49212487..49213629hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582171
Supporting Variants
Samples
Known GenesFOLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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