A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458558



Internal ID21116111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85705965..85719297hg38UCSC Ensembl
chr11:85417008..85430340hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3813333
hg1913333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189838
Samples
Known GenesSYTL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458558
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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