A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259837



Internal ID20469055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38163141..38164538hg38UCSC Ensembl
chr20:36791543..36792940hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741789
Supporting Variants
Samples
Known GenesTGM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259837
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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