A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6251298



Internal ID22055908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18160619..18160619hg38UCSC Ensembl
chr20:18141263..18141263hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17850479
Samples
Known GenesCSRP2BP
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6251298
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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