A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106309



Internal ID22015542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16062087..16190574hg38UCSC Ensembl
chr3:16103594..16232081hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38128488
hg19128488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549467
Samples
Known GenesGALNT15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106309
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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