A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932286



Internal ID22707581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20936787..20956595hg38UCSC Ensembl
chr16:20948109..20967917hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3819809
hg1919809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380426
Samples
Known GenesDNAH3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932286
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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