A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888389



Internal ID22663394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11310783..11310904hg38UCSC Ensembl
chr5:11310895..11311016hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419515
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888389
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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