A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263516



Internal ID20472734
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 StatusS
Merged Variantsnsv4763141
Supporting Variants
Samples
Known GenesKDM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263516
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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