A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107081



Internal ID22016314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153881418..153888074hg38UCSC Ensembl
chr3:153599207..153605863hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg386657
hg196657
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107081
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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