A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5658121



Internal ID21606426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1368918..1368918hg38UCSC Ensembl
chr19:1368917..1368917hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103298
SamplesHG02818
Known GenesMUM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5658121
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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