A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760798



Internal ID20536658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47834676..47896050hg38UCSC Ensembl
chr20:46463420..46524794hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3861375
hg1961375
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv57n199
Supporting Variantsnssv16260181
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760798
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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