A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658951



Internal ID21607256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49379459..49379459hg38UCSC Ensembl
chr16:49413370..49413370hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085430
SamplesNA19239
Known GenesC16orf78
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658951
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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