A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651087



Internal ID21599392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111609102..111609102hg38UCSC Ensembl
chr11:111479826..111479826hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072701
SamplesNA19238
Known GenesSIK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651087
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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