A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104297



Internal ID21493745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3530281..3530446hg38UCSC Ensembl
chr19:3530279..3530444hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603469
Supporting Variants
SamplesNA19238
Known GenesFZR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104297
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer