A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103883



Internal ID21499108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17828456..17828589hg38UCSC Ensembl
chr19:17939265..17939398hg19UCSC 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 Variantsnsv5599391
Supporting Variants
SamplesNA19239
Known GenesJAK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103883
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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