A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734787



Internal ID20510726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75120440..75120617hg38UCSC Ensembl
chr15:75412781..75412958hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734787
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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