A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524189



Internal ID21848547
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 StatusS
Merged Variantsnsv5993543
Supporting Variants
Samples
Known GenesCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524189
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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