A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422544



Internal ID21080097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33422279..33432146hg38UCSC Ensembl
chr8:33279797..33289664hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389868
hg199868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234606
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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