A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196965



Internal ID20764005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98750601..98777900hg38UCSC Ensembl
chr11:98621331..98648630hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3827300
hg1927300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00069


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