A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435832



Internal ID21093385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27088363..27094682hg38UCSC Ensembl
chr11:27109910..27116229hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg386320
hg196320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185112
Samples
Known GenesBBOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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