A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109228



Internal ID22018461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105891460..105893520hg38UCSC Ensembl
chr1:106434082..106436142hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg382061
hg192061
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109228
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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