A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659882



Internal ID21608187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55455873..55455873hg38UCSC Ensembl
chr19:55967240..55967240hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17107022
SamplesHG00731
Known GenesISOC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659882
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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