A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733594



Internal ID20509524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89212795..89212878hg38UCSC Ensembl
chr15:89756026..89756109hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292638
Samples
Known GenesRLBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733594
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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