A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116231



Internal ID21504816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18708207..18708207hg38UCSC Ensembl
chr20:18688851..18688851hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670990
Supporting Variants
SamplesNA19650
Known GenesDTD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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