A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103985



Internal ID21486053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2183926..2183926hg38UCSC Ensembl
chr19:2183925..2183925hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663949
Supporting Variants
SamplesNA12878
Known GenesDOT1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103985
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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