A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105468



Internal ID21498798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4778306..4778306hg38UCSC Ensembl
chr19:4778318..4778318hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646320
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105468
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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