A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105449



Internal ID21402293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47245700..47245700hg38UCSC Ensembl
chr19:47748957..47748957hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650936
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105449
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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