A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140826



Internal ID21466044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140172414..140172471hg38UCSC Ensembl
chr8:141182513..141182570hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576176
Supporting Variants
SamplesHG03065
Known GenesTRAPPC9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140826
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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