A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996560



Internal ID20563600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99419654..99420005hg38UCSC Ensembl
chr11:99290385..99290736hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458358
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00146


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