A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986845



Internal ID20553885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121074649..121075129hg38UCSC Ensembl
chr11:120945358..120945838hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459414
Supporting Variants
Samples
Known GenesTBCEL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00054


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