A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841692



Internal ID22616627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138848823..138855073hg38UCSC Ensembl
chr5:138184512..138190762hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg386251
hg196251
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495563
Samples
Known GenesCTNNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841692
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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