A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767797



Internal ID20543657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46382443..46395373hg38UCSC Ensembl
chr16:46416355..46429285hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3812931
hg1912931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv42n199
Supporting Variantsnssv16295282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767797
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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