A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17108113



Internal ID21441241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119525206..119525206hg38UCSC Ensembl
chr2:120282782..120282782hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624293
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17108113
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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