A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538914



Internal ID20912221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79635233..79635699hg38UCSC Ensembl
chr2:79862359..79862825hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258435
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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