A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441233



Internal ID21098786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109115762..109117308hg38UCSC Ensembl
chr9:111878042..111879588hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381547
hg191547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230198
Samples
Known GenesTMEM245
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441233
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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