A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491499



Internal ID268737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6189013..6189727hg38UCSC Ensembl
chr10:6230976..6231690hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17028965
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491499
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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