A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650983



Internal ID21599288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31586425..31586425hg38UCSC Ensembl
chr19:32077331..32077331hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104386
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650983
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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