A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073321



Internal ID21442145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134046061..134046061hg38UCSC Ensembl
chr11:133915956..133915956hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661771
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073321
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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