A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491145



Internal ID21148698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32027901..32037500hg38UCSC Ensembl
chr13:32602038..32611637hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186522
Samples
Known GenesFRY, FRY-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491145
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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