A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653739



Internal ID21602044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84191990..84191990hg38UCSC Ensembl
chr11:83903033..83903033hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076292
SamplesNA19238
Known GenesDLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653739
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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