A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433284



Internal ID21395286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53468710..53469903hg38UCSC Ensembl
chr20:52085249..52086442hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv458n172
Supporting Variantsnssv15750066
SamplesMDQ045
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433284
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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