A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282966



Internal ID20492184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:161568359..161571984hg38UCSC Ensembl
chr3:161286147..161289772hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg383626
hg193626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282966
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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