A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081363



Internal ID21463000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6083014..6083014hg38UCSC Ensembl
chr16:6133015..6133015hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649762
Supporting Variants
SamplesHG03009
Known GenesRBFOX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081363
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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