A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476019



Internal ID21133572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106033420..106039254hg38UCSC Ensembl
chr13:106685769..106691603hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg385835
hg195835
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476019
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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