A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470527



Internal ID21128080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107853845..107999870hg38UCSC Ensembl
chr11:107724571..107870596hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38146026
hg19146026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185228
Samples
Known GenesRAB39A, SLC35F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470527
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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