A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524557



Internal ID21848915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4084855..4203810hg38UCSC Ensembl
chr3:4126539..4245494hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38118956
hg19118956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524557
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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