A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662764



Internal ID21611069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39413589..39413589hg38UCSC Ensembl
chr19:39904229..39904229hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104712
SamplesNA19650
Known GenesPLEKHG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662764
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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