A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288514



Internal ID20497732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195864483..195864546hg38UCSC Ensembl
chr3:195591354..195591417hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732587
Supporting Variants
Samples
Known GenesTNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288514
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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