A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409721



Internal ID189041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19239130..19239181hg38UCSC Ensembl
chr11:19260677..19260728hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044717
Samples
Known GenesE2F8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409721
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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