A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479283



Internal ID21136836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106327215..106356667hg38UCSC Ensembl
chr13:106979563..107009015hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3829453
hg1929453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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