A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840665



Internal ID22615600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11165654..11177110hg38UCSC Ensembl
chr5:11165766..11177222hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3811457
hg1911457
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493072
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840665
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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