A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104827



Internal ID22014060
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 StatusM
Merged Variants
Supporting Variantsnssv17633012
Samples
Known GenesLINC00494
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104827
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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