A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029337



Internal ID21938680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33131030..33352849hg38UCSC Ensembl
chr11:33152576..33374395hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38221820
hg19221820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596491
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029337
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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