A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763141



Internal ID20539001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67222626..67222626hg38UCSC Ensembl
chr11:66990097..66990097hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263516
Samples
Known GenesKDM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763141
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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