A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596080



Internal ID21544687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19238456..19238523hg38UCSC Ensembl
chr9:19238454..19238521hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161396
SamplesHG00732
Known GenesDENND4C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596080
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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