A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403328



Internal ID22461198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23660088..23660177hg38UCSC Ensembl
chr20:23640725..23640814hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403328
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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