A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112503



Internal ID21503494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241213109..241213109hg38UCSC Ensembl
chr2:242152524..242152524hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613497
Supporting Variants
SamplesNA19239
Known GenesANO7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112503
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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