A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259450



Internal ID20468668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:49907571..49907642hg38UCSC Ensembl
chr20:48524108..48524179hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747266
Supporting Variants
Samples
Known GenesSPATA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259450
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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