A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650156



Internal ID21598461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94882626..94882626hg38UCSC Ensembl
chr11:94615791..94615791hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076853
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650156
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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