A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5647272



Internal ID21595577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97965051..97965051hg38UCSC Ensembl
chr14:98431388..98431388hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098884
SamplesHG01596
Known GenesC14orf64
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5647272
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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