A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650068



Internal ID21598373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39498176..39498176hg38UCSC Ensembl
chr19:39988816..39988816hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104716
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650068
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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