A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074730



Internal ID21446681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46161920..46161920hg38UCSC Ensembl
chr11:46183471..46183471hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662133
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074730
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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