A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662686



Internal ID21610991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56635281..56635281hg38UCSC Ensembl
chr19:57146649..57146649hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106439
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662686
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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