A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653225



Internal ID21601530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30015906..30015906hg38UCSC Ensembl
chr19:30506813..30506813hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104087
SamplesHG03065
Known GenesURI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653225
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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