A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287272



Internal ID20496490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53469526..53469692hg38UCSC Ensembl
chr20:52086065..52086231hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744696
Supporting Variants
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287272
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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