A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102345



Internal ID22011579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162042488..162052885hg38UCSC Ensembl
chr1:162012278..162022675hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102345
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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