A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996565



Internal ID20563605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99485601..99486500hg38UCSC Ensembl
chr11:99356332..99357231hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470201
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00102


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