A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103618



Internal ID21510643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15933105..15933105hg38UCSC Ensembl
chr19:16043915..16043915hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646678
Supporting Variants
SamplesNA24385
Known GenesCYP4F11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103618
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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