A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841016



Internal ID22615951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11819387..11821018hg38UCSC Ensembl
chr5:11819499..11821130hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381632
hg191632
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493754
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841016
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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