A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060295



Internal ID21969529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17828476..17828608hg38UCSC Ensembl
chr19:17939285..17939417hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627715
Samples
Known GenesJAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060295
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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