A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095330



Internal ID21492358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:79395698..79395698hg38UCSC Ensembl
chr12:79789478..79789478hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660562
Supporting Variants
SamplesNA19238
Known GenesSYT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095330
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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