A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013940



Internal ID21923283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138934982..138936221hg38UCSC Ensembl
chr5:138270671..138271910hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540461
Samples
Known GenesCTNNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013940
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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