A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062809



Internal ID21401129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222474050..222474050hg38UCSC Ensembl
chr1:222647392..222647392hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616292
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062809
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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