A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996075



Internal ID20563115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99117269..99122852hg38UCSC Ensembl
chr11:98987999..98993582hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg385584
hg195584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459639
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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