A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076676



Internal ID21403721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94621355..94621355hg38UCSC Ensembl
chr11:94354521..94354521hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646313
Supporting Variants
SamplesHG00171
Known GenesPIWIL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076676
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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