A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147069



Internal ID21422082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22625879..22625879hg38UCSC Ensembl
chr8:22483392..22483392hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639141
Supporting Variants
SamplesHG00731
Known GenesBIN3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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