A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943153



Internal ID22718597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29710118..29730095hg38UCSC Ensembl
chr16:29721439..29741416hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3819978
hg1919978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373818
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943153
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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