A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628350



Internal ID21576655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150173447..150173447hg38UCSC Ensembl
chr5:149553010..149553010hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382047
hg192047
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123325
SamplesNA18534
Known GenesCDX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628350
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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