A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094576



Internal ID21484814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30385461..30385461hg38UCSC Ensembl
chr14:30854667..30854667hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381904
hg191904
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654494
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094576
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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