A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293110



Internal ID20502328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149092058..149093645hg38UCSC Ensembl
chr3:148809845..148811432hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381588
hg191588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739503
Supporting Variants
Samples
Known GenesHLTF-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293110
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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