A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278027



Internal ID20487245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140548761..140550174hg38UCSC Ensembl
chr3:140267603..140269016hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381414
hg191414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743064
Supporting Variants
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278027
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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