A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229705



Internal ID20796745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48563687..49463252hg38UCSC Ensembl
chr11:48585239..49484804hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38899566
hg19899566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584154
Supporting Variants
Samples
Known GenesFOLH1, TRIM49B, TRIM64C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229705
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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