A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979483



Internal ID22754418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65689151..65689151hg38UCSC Ensembl
chr15:65981489..65981489hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371367
Samples
Known GenesDENND4A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979483
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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