A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946705



Internal ID22722200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5491235..5491288hg38UCSC Ensembl
chr20:5471881..5471934hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946705
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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