A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068299



Internal ID21506110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109667037..109667037hg38UCSC Ensembl
chr10:111426795..111426795hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638756
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068299
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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