A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111317



Internal ID22020550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19376563..19385706hg38UCSC Ensembl
chr2:19576324..19585467hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg389144
hg199144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111317
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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