A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027473



Internal ID21936816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118076123..118161781hg38UCSC Ensembl
chr11:117946838..118032496hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3885659
hg1985659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613849
Samples
Known GenesSCN4B, TMPRSS4, TMPRSS4-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027473
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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