A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548223



Internal ID20921419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23941825..23942645hg38UCSC Ensembl
chr2:24164695..24165515hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257452
Samples
Known GenesUBXN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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