A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092205



Internal ID21439172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97431989..97431989hg38UCSC Ensembl
chr14:97898326..97898326hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644700
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092205
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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