A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651128



Internal ID21599433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15271909..15271909hg38UCSC Ensembl
chr19:15382720..15382720hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103613, nssv17103319
SamplesNA19239, NA20509
Known GenesBRD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651128
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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