A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664372



Internal ID21612677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29558009..29558009hg38UCSC Ensembl
chr11:29579556..29579556hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074175
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664372
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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