A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296017



Internal ID20505235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153301225..153301347hg38UCSC Ensembl
chr3:153019014..153019136hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732408
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296017
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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