A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005882



Internal ID21915225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19238465..19238534hg38UCSC Ensembl
chr9:19238463..19238532hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582932
Samples
Known GenesDENND4C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005882
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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