A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105448



Internal ID21498807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47226081..47226081hg38UCSC Ensembl
chr19:47729338..47729338hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664469
Supporting Variants
SamplesNA19239
Known GenesBBC3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105448
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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