A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026907



Internal ID21936250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102601115..102601431hg38UCSC Ensembl
chr11:102471846..102472162hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596282
Samples
Known GenesMMP20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026907
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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