A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448637



Internal ID21106190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103337594..103338080hg38UCSC Ensembl
chr10:105097351..105097837hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977691
Samples
Known GenesPCGF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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