A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945825



Internal ID22721306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65729356..65729444hg38UCSC Ensembl
chr15:66021694..66021782hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383793
Samples
Known GenesDENND4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945825
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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