A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960744



Internal ID22735711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80559889..80559889hg38UCSC Ensembl
chr2:80787014..80787014hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402547
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960744
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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