A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5654313



Internal ID21602618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98330523..98330523hg38UCSC Ensembl
chr14:98796860..98796860hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095060
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5654313
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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