A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033946



Internal ID21943289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47371090..47371385hg38UCSC Ensembl
chr11:47392641..47392936hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594369
Samples
Known GenesSPI1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033946
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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