A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463462



Internal ID22521348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99312789..99314429hg38UCSC Ensembl
chr11:99183520..99185160hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852061
Supporting Variants
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463462
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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