A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754659



Internal ID20530519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16632232..18721508hg38UCSC Ensembl
chr16:16726089..18732830hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382089277
hg192006742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260817
Samples
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8, XYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754659
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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