A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112121



Internal ID22021355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79385304..79528030hg38UCSC Ensembl
chr2:79612430..79755156hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38142727
hg19142727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522133
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112121
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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