A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489548



Internal ID21147101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99607499..99617000hg38UCSC Ensembl
chr13:100259753..100269254hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg389502
hg199502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179600
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489548
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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