A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223668



Internal ID20790708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66702367..66702810hg38UCSC Ensembl
chr11:66469838..66470281hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593271
Supporting Variants
Samples
Known GenesSPTBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223668
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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