A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116462



Internal ID21504176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2115902..2115902hg38UCSC Ensembl
chr20:2096548..2096548hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652007
Supporting Variants
SamplesNA19239
Known GenesSTK35
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116462
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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