A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584735



Internal ID21533278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9394066..9394396hg38UCSC Ensembl
chr16:9487923..9488253hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094400
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584735
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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