A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556192



Internal ID21880547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152081369..152082170hg38UCSC Ensembl
chr3:151799158..151799959hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556192
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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