A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178561



Internal ID20745601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99276209..99341474hg38UCSC Ensembl
chr11:99146940..99212205hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3865266
hg1965266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471775
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178561
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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