A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659691



Internal ID21607996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27517582..27517582hg38UCSC Ensembl
chr11:27539129..27539129hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074129
SamplesHG00513
Known GenesBDNF-AS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659691
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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