A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090096



Internal ID21458114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29399809..29399809hg38UCSC Ensembl
chr14:29869015..29869015hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656022
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090096
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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