A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954568



Internal ID22729803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24437219..24445640hg38UCSC Ensembl
chr20:24417855..24426276hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg388422
hg198422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954568
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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