A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076276



Internal ID21403495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83547561..83547561hg38UCSC Ensembl
chr11:83258604..83258604hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651086
Supporting Variants
SamplesHG00171
Known GenesDLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076276
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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