A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988321



Internal ID20555361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14353058..14356975hg38UCSC Ensembl
chr11:14374604..14378521hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383918
hg193918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445285
Supporting Variants
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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