A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660993



Internal ID21609298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44645128..44645128hg38UCSC Ensembl
chr19:45148437..45148437hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105281
SamplesNA19239
Known GenesPVR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660993
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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