A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731429



Internal ID20507350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56585575..56585721hg38UCSC Ensembl
chr15:56877773..56877919hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731429
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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