A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283474



Internal ID20492692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39290798..39290865hg38UCSC Ensembl
chr3:39332289..39332356hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283474
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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