A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627172



Internal ID21819219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17828388..17828521hg38UCSC Ensembl
chr19:17939197..17939330hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046788
Supporting Variants
Samples
Known GenesJAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627172
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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