A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151747



Internal ID21412320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22293639..22293639hg38UCSC Ensembl
chr6:22293868..22293868hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639319
Supporting Variants
SamplesHG00513
Known GenesPRL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151747
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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