A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905960



Internal ID22681153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11796746..11797559hg38UCSC Ensembl
chr5:11796858..11797671hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418326
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905960
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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