A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897687



Internal ID22672793
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 Variantsnssv17411683
Samples
Known GenesCCNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897687
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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