A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756882



Internal ID20532742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24397274..24406513hg38UCSC Ensembl
chr20:24377910..24387149hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg389240
hg199240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756882
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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