A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586073



Internal ID21534623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6206478..6206602hg38UCSC Ensembl
chr10:6248441..6248565hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071125
SamplesHG02818
Known GenesPFKFB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586073
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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