A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419054



Internal ID21076607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:226434..504317hg38UCSC Ensembl
chr9:226434..504317hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38277884
hg19277884
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231363
Samples
Known GenesDOCK8, KANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419054
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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