A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031022



Internal ID21940365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102685736..102728194hg38UCSC Ensembl
chr11:102556467..102598925hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3842459
hg1942459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597380
Samples
Known GenesMMP27, MMP8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031022
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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