A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109928



Internal ID21488902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195537086..195537086hg38UCSC Ensembl
chr2:196401810..196401810hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620791
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109928
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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