A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937477



Internal ID22712845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84663267..84663633hg38UCSC Ensembl
chr16:84696873..84697239hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384147
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937477
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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