A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428985



Internal ID21086538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19306585..19403955hg38UCSC Ensembl
chr9:19306583..19403953hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3897371
hg1997371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218481
Samples
Known GenesDENND4C, RPS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428985
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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