A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663344



Internal ID21611649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64489699..64489699hg38UCSC Ensembl
chr11:64257171..64257171hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075647
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663344
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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