A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867423



Internal ID22642358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123494050..123495284hg38UCSC Ensembl
chr9:126256329..126257563hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511298
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867423
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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