A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092698



Internal ID21463951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89290381..89290381hg38UCSC Ensembl
chr16:89356789..89356789hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663706
Supporting Variants
SamplesHG03065
Known GenesANKRD11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092698
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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