A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658839



Internal ID21607144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28430912..28430912hg38UCSC Ensembl
chr11:28452459..28452459hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074144
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658839
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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