A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640859



Internal ID21589164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6229149..6229149hg38UCSC Ensembl
chr10:6271112..6271112hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070434
SamplesHG03486
Known GenesPFKFB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640859
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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