A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281806



Internal ID20491024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201211002..201211002hg38UCSC Ensembl
chr1:201180130..201180130hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753250
Supporting Variants
Samples
Known GenesIGFN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281806
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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