A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490559



Internal ID21148112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113956883..114280328hg38UCSC Ensembl
chr13:114739950..115045803hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38323446
hg19305854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189393
Samples
Known GenesCDC16, RASA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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