A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262995



Internal ID20472213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47834673..47894719hg38UCSC Ensembl
chr20:46463417..46523463hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3860047
hg1960047
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262995
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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