A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649327



Internal ID21597632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18283511..18283511hg38UCSC Ensembl
chr11:18305058..18305058hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382809
hg192809
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073844
SamplesHG01505
Known GenesHPS5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649327
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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