A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083830



Internal ID21409900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100026381..100026381hg38UCSC Ensembl
chr14:100492718..100492718hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650024
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083830
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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