A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645405



Internal ID21593710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14841725..14841725hg38UCSC Ensembl
chr11:14863271..14863271hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381063
hg191063
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073213
SamplesHG00731
Known GenesPDE3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645405
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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