A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110034



Internal ID22019267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63702647..63722044hg38UCSC Ensembl
chr16:63736551..63755948hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3819398
hg1919398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110034
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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