A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441766



Internal ID21099319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111763956..111773380hg38UCSC Ensembl
chr9:114526236..114535660hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg389425
hg199425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174614
Samples
Known GenesC9orf84
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441766
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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