A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633821



Internal ID21825868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48929883..48936838hg38UCSC Ensembl
chr19:49433140..49440095hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg386956
hg196956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059241
Supporting Variants
Samples
Known GenesDHDH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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