A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428999



Internal ID21086552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11809194..11816092hg38UCSC Ensembl
chr8:11666703..11673601hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386899
hg196899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227877
Samples
Known GenesFDFT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428999
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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