A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454219



Internal ID21111772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2905224..3284256hg38UCSC Ensembl
chr10:2947416..3326448hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38379033
hg19379033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187120
Samples
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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