A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073686



Internal ID21437778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13791470..13791470hg38UCSC Ensembl
chr11:13813017..13813017hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654505
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073686
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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