A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17546319



Internal ID21870674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154310778..154310832hg38UCSC Ensembl
chr3:154028567..154028621hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992089
Supporting Variants
Samples
Known GenesDHX36
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17546319
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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