A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080442



Internal ID21457919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20310304..20310304hg38UCSC Ensembl
chr14:20778463..20778463hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651447
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080442
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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