A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046788



Internal ID21956021
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 StatusM
Merged Variants
Supporting Variantsnssv17627172
Samples
Known GenesJAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046788
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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