A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626829



Internal ID21818876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49304508..49307044hg38UCSC Ensembl
chr19:49807765..49810301hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg382537
hg192537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050964
Supporting Variants
Samples
Known GenesSLC6A16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626829
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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