A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033252



Internal ID21942595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66685320..66685385hg38UCSC Ensembl
chr11:66452791..66452856hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591740
Samples
Known GenesSPTBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033252
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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