A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747290



Internal ID20523307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77486327..77486422hg38UCSC Ensembl
chr15:77778669..77778764hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747290
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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