A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746691



Internal ID20522705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53417881..53421838hg38UCSC Ensembl
chr15:53710078..53714035hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383958
hg193958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266663
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746691
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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