A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103360



Internal ID21484424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16874386..16874442hg38UCSC Ensembl
chr19:16985197..16985253hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587409
Supporting Variants
SamplesNA12329
Known GenesSIN3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103360
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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