A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235783



Internal ID20802823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113653035..113671915hg38UCSC Ensembl
chr11:113523757..113542637hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3818881
hg1918881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588621
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235783
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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