A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151420



Internal ID21444186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38753905..38753905hg38UCSC Ensembl
chr8:38611423..38611423hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5627738
Supporting Variants
SamplesHG00732
Known GenesTACC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151420
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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