A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267452



Internal ID20476670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120838004..120838138hg38UCSC Ensembl
chr3:120556851..120556985hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267452
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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