A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17114789



Internal ID21460677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67449414..67449414hg38UCSC Ensembl
chr2:67676546..67676546hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612011
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17114789
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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