A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238913



Internal ID20805953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65779033..65779683hg38UCSC Ensembl
chr15:66071371..66072021hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581803
Supporting Variants
Samples
Known GenesDENND4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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