A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272177



Internal ID20481395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27282564..27282564hg38UCSC Ensembl
chr3:27324055..27324055hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757404
Supporting Variants
Samples
Known GenesNEK10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272177
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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