A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731506



Internal ID20507427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53328573..53328648hg38UCSC Ensembl
chr13:53902708..53902783hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731506
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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