A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090552



Internal ID21408508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57159099..57159099hg38UCSC Ensembl
chr14:57625817..57625817hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664138
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090552
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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