A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598828



Internal ID21547457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29554013..29554326hg38UCSC Ensembl
chr16:29565334..29565647hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088541
SamplesHG00732
Known GenesLOC440354
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598828
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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