A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653393



Internal ID21601698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64366904..64366904hg38UCSC Ensembl
chr11:64134376..64134376hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381495
hg191495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075645
SamplesHG02492
Known GenesRPS6KA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653393
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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