A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446042



Internal ID21103595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113412441..113418676hg38UCSC Ensembl
chr9:116174721..116180956hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg386236
hg196236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174394
Samples
Known GenesC9orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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