A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662360



Internal ID21610665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8896151..8896151hg38UCSC Ensembl
chr19:9006827..9006827hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106787
SamplesHG00171
Known GenesMUC16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662360
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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