A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650263



Internal ID21598568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13953690..13953690hg38UCSC Ensembl
chr16:14047547..14047547hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094862
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650263
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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