A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420466



Internal ID21078019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48663945..48670353hg38UCSC Ensembl
chr8:49576505..49582913hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg386409
hg196409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233195
Samples
Known GenesLOC101929268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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