A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218220



Internal ID20785260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118393135..118393599hg38UCSC Ensembl
chr11:118263850..118264314hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577191
Supporting Variants
Samples
Known GenesLOC100131626, UBE4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218220
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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