A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657523



Internal ID21605828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84099878..84099878hg38UCSC Ensembl
chr11:83810921..83810921hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076287
SamplesHG00513
Known GenesDLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657523
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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