A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251182



Internal ID22055792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3261772..3261772hg38UCSC Ensembl
chr20:3242418..3242418hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850352
Samples
Known GenesC20orf194
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251182
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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