A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649967



Internal ID21598272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91052211..91052211hg38UCSC Ensembl
chr14:91518555..91518555hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086486
SamplesHG00732
Known GenesRPS6KA5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649967
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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