A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733895



Internal ID20509827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92768544..92768696hg38UCSC Ensembl
chr15:93311774..93311926hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733895
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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