A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17624028



Internal ID21816075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53634153..53640317hg38UCSC Ensembl
chr19:54137407..54143571hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386165
hg196165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050248
Supporting Variants
Samples
Known GenesDPRX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17624028
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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