A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993543



Internal ID21902886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:262070..262387hg38UCSC Ensembl
chr3:303753..304070hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524189
Samples
Known GenesCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993543
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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