A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734145



Internal ID20510079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32974273..32974402hg38UCSC Ensembl
chr1:33439874..33440003hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734145
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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