A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574013



Internal ID21522424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69175268..69175321hg38UCSC Ensembl
chr5:68471095..68471148hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154588
SamplesHG01114
Known GenesCCNB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574013
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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