A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582932



Internal ID21774975
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 StatusS
Merged Variantsnsv6005882
Supporting Variants
Samples
Known GenesDENND4C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582932
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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