A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850666



Internal ID22034309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58256036..58256036hg38UCSC Ensembl
chr20:56831092..56831092hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251567
Supporting Variants
Samples
Known GenesPPP4R1L
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850666
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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