A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928338



Internal ID22703575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29256852..29256932hg38UCSC Ensembl
chr16:29268173..29268253hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928338
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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