A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624353



Internal ID21816400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48592207..48593450hg38UCSC Ensembl
chr19:49095464..49096707hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381244
hg191244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043670
Supporting Variants
Samples
Known GenesSULT2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624353
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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