A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072921



Internal ID21440230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122406923..122406923hg38UCSC Ensembl
chr11:122277631..122277631hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655528
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072921
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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