A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096263



Internal ID21454820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23110684..23110684hg38UCSC Ensembl
chr14:23579893..23579893hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655843
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096263
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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