A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920818



Internal ID22696041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6231829..6231891hg38UCSC Ensembl
chr10:6273792..6273854hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356806
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920818
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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