A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227808



Internal ID20794848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59818088..59818224hg38UCSC Ensembl
chr11:59585561..59585697hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593946
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227808
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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