A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259342



Internal ID20468560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:123517905..123518220hg38UCSC Ensembl
chr3:123236752..123237067hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748661
Supporting Variants
Samples
Known GenesPTPLB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259342
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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