A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262494



Internal ID20471712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38081363..38081714hg38UCSC Ensembl
chr3:38122854..38123205hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747238
Supporting Variants
Samples
Known GenesDLEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262494
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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