A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426659



Internal ID21084212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86622..258649hg38UCSC Ensembl
chr9:86622..258649hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38172028
hg19172028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7532n223
Supporting Variantsnssv18178923
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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