A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589989



Internal ID21782032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33880254..33880254hg38UCSC Ensembl
chr11:33901800..33901800hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087488
Supporting Variants
Samples
Known GenesLMO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589989
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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