A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105388



Internal ID21481861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4533141..4536453hg38UCSC Ensembl
chr19:4533153..4536465hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383313
hg193313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600464
Supporting Variants
SamplesHG03683
Known GenesPLIN5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105388
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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