A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219429



Internal ID20786469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21691902..21833135hg38UCSC Ensembl
chr11:21713448..21854681hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38141234
hg19141234
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219429
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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