A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632867



Internal ID21581172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59172045..59172045hg38UCSC Ensembl
chr5:58467871..58467871hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155101
SamplesHG02011
Known GenesPDE4D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632867
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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