A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087359



Internal ID21996592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132744958..132744958hg38UCSC Ensembl
chr11:132614853..132614853hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604901
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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