A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089926



Internal ID21440346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54562154..54562154hg38UCSC Ensembl
chr14:55028872..55028872hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653382
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089926
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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