A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103797



Internal ID21493662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11425132..11425132hg38UCSC Ensembl
chr19:11536029..11536029hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657831
Supporting Variants
SamplesNA19238
Known GenesCCDC151
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103797
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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