A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935174



Internal ID22710512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64838754..64838861hg38UCSC Ensembl
chr16:64872657..64872764hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935174
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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