A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996589



Internal ID20563629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99650416..99776358hg38UCSC Ensembl
chr11:99521147..99647089hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38125943
hg19125943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460596
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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