A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857596



Internal ID22632531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123494051..123497909hg38UCSC Ensembl
chr9:126256330..126260188hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511299
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857596
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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