A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424185



Internal ID21081738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98236..518063hg38UCSC Ensembl
chr9:98236..518063hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38419828
hg19419828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221597
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4, KANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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