A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147611



Internal ID21401872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139804354..139804354hg38UCSC Ensembl
chr8:140816597..140816597hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644128
Supporting Variants
SamplesHG00096
Known GenesTRAPPC9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147611
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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