A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062851



Internal ID21506497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226466698..226466698hg38UCSC Ensembl
chr1:226654399..226654399hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624215
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062851
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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