A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762997



Internal ID20538857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47894719..48503213hg38UCSC Ensembl
chr20:46523463..47131459hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38608495
hg19607997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287774
Samples
Known GenesLINC00494
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762997
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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