A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217949



Internal ID20784989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119245161..119245487hg38UCSC Ensembl
chr11:119115871..119116197hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580917
Supporting Variants
Samples
Known GenesCBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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