A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740293



Internal ID20516268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91304248..91304312hg38UCSC Ensembl
chr15:91847478..91847542hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740293
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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