A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633012



Internal ID21825059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47894718..48509792hg38UCSC Ensembl
chr20:46523462..47131704hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38615075
hg19608243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104827
Supporting Variants
Samples
Known GenesLINC00494
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633012
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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