A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231774



Internal ID20798814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102129546..102129860hg38UCSC Ensembl
chr11:102000277..102000591hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593409
Supporting Variants
Samples
Known GenesYAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231774
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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