A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738548



Internal ID20514518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19238443..19238576hg38UCSC Ensembl
chr9:19238441..19238574hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290541
Samples
Known GenesDENND4C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738548
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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