A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409306



Internal ID21066859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11414201..11421800hg38UCSC Ensembl
chr6:11414434..11422033hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409306
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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