A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022949



Internal ID21932292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94057397..94077603hg38UCSC Ensembl
chr11:93790563..93810769hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3820207
hg1920207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588840
Samples
Known GenesHEPHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022949
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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